Fosinopril sodium
- Product NDC
- 50268-328
- 11-digit product format
- 502680328
- Labeler code
- 50268
- Product ID
- 50268-328_d5cf6c40-2db7-c82a-e053-2a95a90a9aa8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fosinopril sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA205670
- Marketing category
- ANDA
- Marketing start
- 2020-08-12
- 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
- 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 |
|---|
| 50268-328-15 | 50268032815 | 50 BLISTER PACK in 1 BOX (50268-328-15) > 1 TABLET in 1 BLISTER PACK (50268-328-11) | 50 blister pack | 2020-08-12 | 0000-00-00 | No | No | Current |