Fosinopril sodium
- Product NDC
- 50090-3428
- 11-digit product format
- 500903428
- Labeler code
- 50090
- Product ID
- 50090-3428_c012fe48-c5e9-4334-a16f-9b4a141217d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2005-06-21
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 40 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