NDC properties for "Betimol 0.5 % Ophthalmic Solution" (RxCUI 1992305)
About this data
The tables show NDC propoerties for Betimol 0.5 % Ophthalmic Solution with the RxCUI 1992305
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for Betimol 0.5 % Ophthalmic Solution (RxCUI 1992305)
| MMSL_CODE | BD3325 |
|---|---|
| NDA | NDA020439 |
| RxCUI | 1992305 |
| SPL_SET_ID | 00f62dd1-dad2-4892-8a5d-21e5e54509ce |
| SPL_SET_ID | 3ae775f4-340c-4bf4-aa49-8a31daba0f8b |
| SPL_SET_ID | 3d7acd55-33b1-4a24-99ae-01f87b0dca1f |
| Prescribable Synonym | BETIMOL 0.5 % Ophthalmic Solution |
| RXNAV_STR | Betimol 0.5 % Ophthalmic Solution |
| RxNorm Name | timolol hemihydrate 5 MG/ML Ophthalmic Solution [Betimol] |
| RxNorm Synonym | Betimol 0.5 % Ophthalmic Solution |
| RxNorm Synonym | Betimol 5 MG/ML (as timolol hemihydrate 5.12 MG/ML) Ophthalmic Solution |
| Related queries | Interactions (for RxCUI 1992305) |
NDC Properties
NDC Item 76478000205
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-05 |
| NDC Item | 76478000205 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-05) / 5 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000210
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-10 |
| NDC Item | 76478000210 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-10) / 10 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000215
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-15 |
| NDC Item | 76478000215 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-15) / 15 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 82584000205
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-05 |
| NDC Item | 82584000205 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 82584000215
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-15 |
| NDC Item | 82584000215 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-15) / 15 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 76478000205
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-05 |
| NDC Item | 76478000205 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-05) / 5 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000210
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-10 |
| NDC Item | 76478000210 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-10) / 10 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000215
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-15 |
| NDC Item | 76478000215 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-15) / 15 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 82584000205
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-05 |
| NDC Item | 82584000205 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 82584000215
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-15 |
| NDC Item | 82584000215 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-15) / 15 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 76478000205
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-05 |
| NDC Item | 76478000205 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-05) / 5 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000210
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-10 |
| NDC Item | 76478000210 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-10) / 10 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000215
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-15 |
| NDC Item | 76478000215 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-15) / 15 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 82584000205
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-05 |
| NDC Item | 82584000205 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 82584000215
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-15 |
| NDC Item | 82584000215 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-15) / 15 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 76478000205
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-05 |
| NDC Item | 76478000205 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-05) / 5 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000210
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-10 |
| NDC Item | 76478000210 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-10) / 10 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000215
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-15 |
| NDC Item | 76478000215 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-15) / 15 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 82584000205
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-05 |
| NDC Item | 82584000205 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 82584000215
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-15 |
| NDC Item | 82584000215 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-15) / 15 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 76478000205
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-05 |
| NDC Item | 76478000205 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-05) / 5 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000210
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-10 |
| NDC Item | 76478000210 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-10) / 10 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 76478000215
| NDC 9 | 76478-002 |
|---|---|
| NDC 10 | 76478-002-15 |
| NDC Item | 76478000215 |
| Packaging | 1 BOTTLE in 1 CARTON (76478-002-15) / 15 mL in 1 BOTTLE |
| FDA SPL set id | 636406 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-01-02 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 76478-002 |
NDC Item 82584000205
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-05 |
| NDC Item | 82584000205 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-05) / 5 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |
NDC Item 82584000215
| NDC 9 | 82584-002 |
|---|---|
| NDC 10 | 82584-002-15 |
| NDC Item | 82584000215 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-002-15) / 15 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783305 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-15 |
| Marketing status | ACTIVE |
| NDA | NDA020439 |
| Related queries | Properties for NDC 9 82584-002 |