Fosinopril Sodium
- Product NDC
- 68788-7717
- 11-digit product format
- 687887717
- Labeler code
- 68788
- Product ID
- 68788-7717_31ebef0f-0c0f-4d17-8da2-16a5fa56b05c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2020-06-01
- 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
- 2023-12-31
- 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 |
|---|
| 68788-7717-1 | 68788771701 | 100 TABLET in 1 BOTTLE (68788-7717-1) | 100 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7717-3 | 68788771703 | 30 TABLET in 1 BOTTLE (68788-7717-3) | 30 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7717-6 | 68788771706 | 60 TABLET in 1 BOTTLE (68788-7717-6) | 60 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7717-9 | 68788771709 | 90 TABLET in 1 BOTTLE (68788-7717-9) | 90 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |