Sucralfate
- Product NDC
- 45865-845
- 11-digit product format
- 458650845
- Labeler code
- 45865
- Product ID
- 45865-845_7e04552c-4601-e0e2-e053-2991aa0a358e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 1996-11-11
- Marketing end
- 2020-04-30
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC],Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record