NDC properties for "Carafate 1000 MG Oral Tablet" (RxCUI 208097)
About this data
The tables show NDC propoerties for Carafate 1000 MG Oral Tablet with the RxCUI 208097
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 1000 MG Oral Tablet (RxCUI 208097)
| MMSL_CODE | BD2991 |
|---|---|
| NDA | NDA018333 |
| RxCUI | 208097 |
| SPL_SET_ID | c87c6b50-6977-4fa7-ae98-40c0753f7aee |
| Prescribable Synonym | Carafate 1 GM Oral Tablet |
| RXNAV_STR | Carafate 1000 MG Oral Tablet |
| RxNorm Name | sucralfate 1000 MG Oral Tablet [Carafate] |
| RxNorm Synonym | Carafate 1000 MG Oral Tablet |
| Related queries | Interactions (for RxCUI 208097) |
NDC Properties
NDC Item 00247124506
| NDC 9 | 0247-1245 |
|---|---|
| NDC 10 | 0247-1245-06 |
| NDC Item | 00247124506 |
| Related queries | Properties for NDC 9 0247-1245 |
NDC Item 52959005230
| NDC 9 | 52959-052 |
|---|---|
| NDC 10 | 52959-052-30 |
| NDC Item | 52959005230 |
| Related queries | Properties for NDC 9 52959-052 |
NDC Item 58914017110
| NDC 9 | 58914-171 |
|---|---|
| NDC 10 | 58914-171-10 |
| NDC Item | 58914017110 |
| Packaging | 100 TABLET in 1 BOTTLE (58914-171-10) |
| COLORTEXT | PINK(Light pink) |
| Color | C48328 __ |
| FDA SPL set id | 483118 |
| Imprint code | CARAFATE;1712 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1981-10-30 |
| Marketing status | ACTIVE |
| NDA | NDA018333 |
| Score | 2 |
| Shapetext | Oblong |
| Shape | C48345 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 58914-171 |
NDC Item 00247124506
| NDC 9 | 0247-1245 |
|---|---|
| NDC 10 | 0247-1245-06 |
| NDC Item | 00247124506 |
| Related queries | Properties for NDC 9 0247-1245 |
NDC Item 52959005230
| NDC 9 | 52959-052 |
|---|---|
| NDC 10 | 52959-052-30 |
| NDC Item | 52959005230 |
| Related queries | Properties for NDC 9 52959-052 |
NDC Item 58914017110
| NDC 9 | 58914-171 |
|---|---|
| NDC 10 | 58914-171-10 |
| NDC Item | 58914017110 |
| Packaging | 100 TABLET in 1 BOTTLE (58914-171-10) |
| COLORTEXT | PINK(Light pink) |
| Color | C48328 __ |
| FDA SPL set id | 483118 |
| Imprint code | CARAFATE;1712 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1981-10-30 |
| Marketing status | ACTIVE |
| NDA | NDA018333 |
| Score | 2 |
| Shapetext | Oblong |
| Shape | C48345 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 58914-171 |
NDC Item 00247124506
| NDC 9 | 0247-1245 |
|---|---|
| NDC 10 | 0247-1245-06 |
| NDC Item | 00247124506 |
| Related queries | Properties for NDC 9 0247-1245 |
NDC Item 52959005230
| NDC 9 | 52959-052 |
|---|---|
| NDC 10 | 52959-052-30 |
| NDC Item | 52959005230 |
| Related queries | Properties for NDC 9 52959-052 |
NDC Item 58914017110
| NDC 9 | 58914-171 |
|---|---|
| NDC 10 | 58914-171-10 |
| NDC Item | 58914017110 |
| Packaging | 100 TABLET in 1 BOTTLE (58914-171-10) |
| COLORTEXT | PINK(Light pink) |
| Color | C48328 __ |
| FDA SPL set id | 483118 |
| Imprint code | CARAFATE;1712 |
| Labeler | Allergan, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1981-10-30 |
| Marketing status | ACTIVE |
| NDA | NDA018333 |
| Score | 2 |
| Shapetext | Oblong |
| Shape | C48345 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 58914-171 |