Sucralfate
- Product NDC
- 63629-6535
- 11-digit product format
- 636296535
- Labeler code
- 63629
- Product ID
- 63629-6535_8bb983c2-9e38-4e3d-9c8c-74e0229b94a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018333
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1996-11-01
- Marketing end
- 0000-00-00
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC],Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63629-6535-1 | 2021-04-26 | C162847 | 48780-1 | 9d75b9d0-565c-f424-e053-dadaa90a57ce | acc107a2-f8c1-4055-97f2-660a8ca2eeb5 |
| 63629-6535-2 | 2021-04-26 | C162847 | 48780-1 | 9d75b9d0-565c-f424-e053-dadaa90a57ce | acc107a2-f8c1-4055-97f2-660a8ca2eeb5 |
| 63629-6535-3 | 2021-04-26 | C162847 | 48780-1 | 9d75b9d0-565c-f424-e053-dadaa90a57ce | acc107a2-f8c1-4055-97f2-660a8ca2eeb5 |
| 63629-6535-4 | 2021-04-26 | C162847 | 48780-1 | 9d75b9d0-565c-f424-e053-dadaa90a57ce | acc107a2-f8c1-4055-97f2-660a8ca2eeb5 |
| 63629-6535-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-565c-f424-e053-dadaa90a57ce | acc107a2-f8c1-4055-97f2-660a8ca2eeb5 |
| 63629-6535-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-565c-f424-e053-dadaa90a57ce | acc107a2-f8c1-4055-97f2-660a8ca2eeb5 |
| 63629-6535-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-565c-f424-e053-dadaa90a57ce | acc107a2-f8c1-4055-97f2-660a8ca2eeb5 |
| 63629-6535-4 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-565c-f424-e053-dadaa90a57ce | acc107a2-f8c1-4055-97f2-660a8ca2eeb5 |