Sucralfate
- Product NDC
- 0591-3892
- 11-digit product format
- 005913892
- Labeler code
- 0591
- Product ID
- 0591-3892_d2c32e6d-08f1-43bc-af9c-5e9b086f7b72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 2016-12-05
- 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
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 01e96ee1-fe82-0132-025c-ec1559bf8b6e | Product name | 5 | 20260127 |
| f9fa5fa8-e047-2182-3e2c-c4a9ec6531cd | Product name | 3 | 20240508 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0591-3892-01 | EA - Each | 0591-3892 | c1ef23e6-d0f5-4dd9-849e-7f6c2d66623a | 1 | 2017-03-06 |
| 0591-3892-05 | EA - Each | 0591-3892 | d1e04b36-9a97-4bc1-854b-159e13663ffb | 1 | 2017-03-06 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 314234 | sucralfate 1 GM Oral Tablet | PSN | bc0d5372-4445-492a-9e7b-5493951143a7 | 2 |
| 314234 | sucralfate 1000 MG Oral Tablet | SCD | bc0d5372-4445-492a-9e7b-5493951143a7 | 2 |
| 314234 | sucralfate 1 GM Oral Tablet | SY | bc0d5372-4445-492a-9e7b-5493951143a7 | 2 |