Fosinopril sodium
- Product NDC
- 68788-7333
- 11-digit product format
- 687887333
- Labeler code
- 68788
- Product ID
- 68788-7333_020987fc-10d1-4b92-abcd-9dde4623aba5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fosinopril sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA205670
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7333-1 | 68788733301 | 100 TABLET in 1 BOTTLE (68788-7333-1) | 100 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7333-3 | 68788733303 | 30 TABLET in 1 BOTTLE (68788-7333-3) | 30 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7333-6 | 68788733306 | 60 TABLET in 1 BOTTLE (68788-7333-6) | 60 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7333-9 | 68788733309 | 90 TABLET in 1 BOTTLE (68788-7333-9) | 90 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |