NDC properties for "Carafate 1 GM per 10 ML Oral Suspension" (RxCUI 208094)
About this data
The tables show NDC propoerties for Carafate 1 GM per 10 ML Oral Suspension with the RxCUI 208094
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 Carafate 1 GM per 10 ML Oral Suspension (RxCUI 208094)
| MMSL_CODE | BD2989 |
|---|---|
| NDA | NDA019183 |
| RxCUI | 208094 |
| SPL_SET_ID | 0bd18d2a-07b3-4155-b08a-bdd0cfd0bd2e |
| SPL_SET_ID | 0fb67b1c-b4c0-46f2-8a81-df1510e006aa |
| SPL_SET_ID | 64ae3d08-5651-463e-a255-9004100433e7 |
| Prescribable Synonym | Carafate 1 GM in 10 mL Oral Suspension |
| RXNAV_STR | Carafate 100 MG/ML Oral Suspension |
| RxNorm Name | sucralfate 100 MG/ML Oral Suspension [Carafate] |
| RxNorm Synonym | Carafate 1 GM per 10 ML Oral Suspension |
| RxNorm Synonym | Carafate 100 MG/ML Oral Suspension |
| Related queries | Interactions (for RxCUI 208094) |
NDC Properties
NDC Item 58914017014
| NDC 9 | 58914-170 |
|---|---|
| NDC 10 | 58914-170-14 |
| NDC Item | 58914017014 |
| Packaging | 420 mL in 1 BOTTLE (58914-170-14) |
| COLORTEXT | pink |
| Color | C48328 __ |
| FDA SPL set id | 769334 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1993-12-16 |
| Marketing status | ACTIVE |
| NDA | NDA019183 |
| Related queries | Properties for NDC 9 58914-170 |
NDC Item 58914017060
| NDC 9 | 58914-170 |
|---|---|
| NDC 10 | 58914-170-60 |
| NDC Item | 58914017060 |
| Packaging | 6 CUP, UNIT-DOSE in 1 BOX (58914-170-60) / 10 mL in 1 CUP, UNIT-DOSE |
| COLORTEXT | pink |
| Color | C48328 __ |
| FDA SPL set id | 769334 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1993-12-16 |
| Marketing status | ACTIVE |
| NDA | NDA019183 |
| Related queries | Properties for NDC 9 58914-170 |
NDC Item 58914017014
| NDC 9 | 58914-170 |
|---|---|
| NDC 10 | 58914-170-14 |
| NDC Item | 58914017014 |
| Packaging | 420 mL in 1 BOTTLE (58914-170-14) |
| COLORTEXT | pink |
| Color | C48328 __ |
| FDA SPL set id | 769334 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1993-12-16 |
| Marketing status | ACTIVE |
| NDA | NDA019183 |
| Related queries | Properties for NDC 9 58914-170 |
NDC Item 58914017060
| NDC 9 | 58914-170 |
|---|---|
| NDC 10 | 58914-170-60 |
| NDC Item | 58914017060 |
| Packaging | 6 CUP, UNIT-DOSE in 1 BOX (58914-170-60) / 10 mL in 1 CUP, UNIT-DOSE |
| COLORTEXT | pink |
| Color | C48328 __ |
| FDA SPL set id | 769334 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1993-12-16 |
| Marketing status | ACTIVE |
| NDA | NDA019183 |
| Related queries | Properties for NDC 9 58914-170 |