Sucralfate
- Product NDC
- 63629-7957
- 11-digit product format
- 636297957
- Labeler code
- 63629
- Product ID
- 63629-7957_38ad6fa2-eae7-463f-a46c-b0c1b4988eda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 1996-11-11
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record