CAPTOPRIL
- Product NDC
- 68788-9721
- 11-digit product format
- 687889721
- Labeler code
- 68788
- Product ID
- 68788-9721_dd99e922-e9a7-4274-a190-2f581a104ba4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA074532
- Marketing category
- ANDA
- Marketing start
- 2012-12-13
- Marketing end
- 0000-00-00
- Substance
- CAPTOPRIL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record