NDC properties for "Equisul SDT (sulfadiazine 333 MG/ML / trimethoprim 67 MG/ML) Oral Suspension" (RxCUI 1592912)
About this data
The tables show NDC propoerties for Equisul SDT (sulfadiazine 333 MG/ML / trimethoprim 67 MG/ML) Oral Suspension with the RxCUI 1592912
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 Equisul SDT (sulfadiazine 333 MG/ML / trimethoprim 67 MG/ML) Oral Suspension (RxCUI 1592912)
| NADA | NADA141360 |
|---|---|
| RxCUI | 1592912 |
| SPL_SET_ID | 434cfb08-bb19-46fc-a55d-b9ecf0bec601 |
| Prescribable Synonym | Equisul SDT 333 MG/mL / 67 MG/mL Oral Suspension |
| RXNAV_STR | sulfADIAZINE 333 MG/ML / TMP 67 MG/ML Oral Suspension [Equisul SDT] |
| RxNorm Name | sulfadiazine 333 MG/ML / trimethoprim 67 MG/ML Oral Suspension [Equisul SDT] |
| RxNorm Synonym | Equisul SDT (sulfadiazine 333 MG/ML / trimethoprim 67 MG/ML) Oral Suspension |
| RxNorm Synonym | Equisul SDT (sulfadiazine 333 MG/ML / trimethoprim 67 MG/ML) per ML Oral Suspension |
| RxNorm Synonym | Sulfadiazine 333 MG/ML / TMP 67 MG/ML Oral Suspension [Equisul SDT] |
| Tallman Synonym | Equisul SDT (sulfADIAZINE 333 MG/ML / trimethoprim 67 MG/ML) Oral Suspension |
| Tallman Synonym | Equisul SDT (sulfADIAZINE 333 MG/ML / trimethoprim 67 MG/ML) per ML Oral Suspension |
| Tallman Synonym | sulfADIAZINE 333 MG/ML / TMP 67 MG/ML Oral Suspension [Equisul SDT] |
| Tallman Synonym | sulfADIAZINE 333 MG/ML / trimethoprim 67 MG/ML Oral Suspension [Equisul SDT] |
| Related queries | Interactions (for RxCUI 1592912) |
NDC Properties
NDC Item 51072002000
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-00 |
| NDC Item | 51072002000 |
| Packaging | 900 mL in 1 BOTTLE (51072-020-00) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002001
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-01 |
| NDC Item | 51072002001 |
| Packaging | 135 mL in 1 BOTTLE (51072-020-01) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002002
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-02 |
| NDC Item | 51072002002 |
| Packaging | 560 mL in 1 BOTTLE (51072-020-02) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002003
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-03 |
| NDC Item | 51072002003 |
| Packaging | 280 mL in 1 BOTTLE (51072-020-03) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002000
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-00 |
| NDC Item | 51072002000 |
| Packaging | 900 mL in 1 BOTTLE (51072-020-00) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002001
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-01 |
| NDC Item | 51072002001 |
| Packaging | 135 mL in 1 BOTTLE (51072-020-01) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002002
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-02 |
| NDC Item | 51072002002 |
| Packaging | 560 mL in 1 BOTTLE (51072-020-02) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002003
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-03 |
| NDC Item | 51072002003 |
| Packaging | 280 mL in 1 BOTTLE (51072-020-03) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002000
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-00 |
| NDC Item | 51072002000 |
| Packaging | 900 mL in 1 BOTTLE (51072-020-00) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002001
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-01 |
| NDC Item | 51072002001 |
| Packaging | 135 mL in 1 BOTTLE (51072-020-01) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002002
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-02 |
| NDC Item | 51072002002 |
| Packaging | 560 mL in 1 BOTTLE (51072-020-02) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002003
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-03 |
| NDC Item | 51072002003 |
| Packaging | 280 mL in 1 BOTTLE (51072-020-03) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002000
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-00 |
| NDC Item | 51072002000 |
| Packaging | 900 mL in 1 BOTTLE (51072-020-00) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002001
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-01 |
| NDC Item | 51072002001 |
| Packaging | 135 mL in 1 BOTTLE (51072-020-01) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002002
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-02 |
| NDC Item | 51072002002 |
| Packaging | 560 mL in 1 BOTTLE (51072-020-02) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |
NDC Item 51072002003
| NDC 9 | 51072-020 |
|---|---|
| NDC 10 | 51072-020-03 |
| NDC Item | 51072002003 |
| Packaging | 280 mL in 1 BOTTLE (51072-020-03) |
| COLORTEXT | WHITE |
| Color | C48325 __ |
| FDA SPL set id | 604389 |
| Labeler | Aurora Pharmaceutical, Inc., DBA Jefferson Labs |
| Label type | PRESCRIPTION ANIMAL DRUG |
| Marketing category | NADA |
| Marketing effective time low | 2013-08-05 |
| Marketing status | ACTIVE |
| NADA | NADA141360 |
| Related queries | Properties for NDC 9 51072-020 |