Fosinopril Sodium
- Product NDC
- 16571-772
- 11-digit product format
- 165710772
- Labeler code
- 16571
- Product ID
- 16571-772_b472fd01-b492-4399-967d-ddfd4bb98faa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- ANDA091163
- Marketing category
- ANDA
- Marketing start
- 2011-03-30
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 16571-772-09 | 16571077209 | 90 TABLET in 1 BOTTLE (16571-772-09) | 90 tablet | 2011-03-30 | 0000-00-00 | No | No | Current |
| 16571-772-10 | 16571077210 | 1000 TABLET in 1 BOTTLE (16571-772-10) | 1000 tablet | 2011-03-30 | 0000-00-00 | No | No | Current |