NDC properties for "Tetravisc 0.5 % Ophthalmic Solution" (RxCUI 1547777)
About this data
The tables show NDC propoerties for Tetravisc 0.5 % Ophthalmic Solution with the RxCUI 1547777
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 Tetravisc 0.5 % Ophthalmic Solution (RxCUI 1547777)
| MMSL_CODE | BD3004 |
|---|---|
| RxCUI | 1547777 |
| Prescribable Synonym | TetraVisc 0.5 % Ophthalmic Solution |
| RXNAV_STR | Tetravisc 0.5 % Ophthalmic Solution |
| RxNorm Name | tetracaine hydrochloride 5 MG/ML Ophthalmic Solution [Tetravisc] |
| RxNorm Synonym | Tetravisc 0.5 % Ophthalmic Solution |
| RxNorm Synonym | Tetravisc 25 MG per 5 ML Ophthalmic Solution |
| Related queries | Interactions (for RxCUI 1547777) |
NDC Properties
NDC Item 54799050401
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-01 |
| NDC Item | 54799050401 |
| Packaging | .6 mL in 1 BOTTLE, DROPPER (54799-504-01) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-504 |
NDC Item 54799050405
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-05 |
| NDC Item | 54799050405 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (54799-504-05) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-504 |
NDC Item 54799050501
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-01 |
| NDC Item | 54799050501 |
| Packaging | .6 mL in 1 BOTTLE, DROPPER (54799-505-01) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-505 |
NDC Item 54799050505
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-05 |
| NDC Item | 54799050505 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (54799-505-05) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-505 |
NDC Item 54799050401
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-01 |
| NDC Item | 54799050401 |
| Packaging | .6 mL in 1 BOTTLE, DROPPER (54799-504-01) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-504 |
NDC Item 54799050405
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-05 |
| NDC Item | 54799050405 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (54799-504-05) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-504 |
NDC Item 54799050501
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-01 |
| NDC Item | 54799050501 |
| Packaging | .6 mL in 1 BOTTLE, DROPPER (54799-505-01) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-505 |
NDC Item 54799050505
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-05 |
| NDC Item | 54799050505 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (54799-505-05) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-505 |
NDC Item 54799050401
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-01 |
| NDC Item | 54799050401 |
| Packaging | .6 mL in 1 BOTTLE, DROPPER (54799-504-01) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-504 |
NDC Item 54799050405
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-05 |
| NDC Item | 54799050405 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (54799-504-05) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-504 |
NDC Item 54799050501
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-01 |
| NDC Item | 54799050501 |
| Packaging | .6 mL in 1 BOTTLE, DROPPER (54799-505-01) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-505 |
NDC Item 54799050505
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-05 |
| NDC Item | 54799050505 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (54799-505-05) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-505 |
NDC Item 54799050401
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-01 |
| NDC Item | 54799050401 |
| Packaging | .6 mL in 1 BOTTLE, DROPPER (54799-504-01) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-504 |
NDC Item 54799050405
| NDC 9 | 54799-504 |
|---|---|
| NDC 10 | 54799-504-05 |
| NDC Item | 54799050405 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (54799-504-05) |
| FDA SPL set id | 363279 |
| FDA SPL set id | 376018 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2009-08-25 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-504 |
NDC Item 54799050501
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-01 |
| NDC Item | 54799050501 |
| Packaging | .6 mL in 1 BOTTLE, DROPPER (54799-505-01) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-505 |
NDC Item 54799050505
| NDC 9 | 54799-505 |
|---|---|
| NDC 10 | 54799-505-05 |
| NDC Item | 54799050505 |
| Packaging | 5 mL in 1 BOTTLE, DROPPER (54799-505-05) |
| FDA SPL set id | 363452 |
| Labeler | OCuSOFT, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing effective time high | 2019-07-16 |
| Marketing effective time low | 2005-08-02 |
| Marketing status | COMPLETED |
| UNAPPROVED_DRUG_OTHER | N/A |
| Related queries | Properties for NDC 9 54799-505 |