Fosinopril Sodium
- Product NDC
- 63629-6994
- 11-digit product format
- 636296994
- Labeler code
- 63629
- Product ID
- 63629-6994_9bc9afaf-6cda-457e-a9c1-0304137239dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2007-09-17
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6994-1 | 63629699401 | 30 TABLET in 1 BOTTLE (63629-6994-1) | 30 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |
| 63629-6994-2 | 63629699402 | 28 TABLET in 1 BOTTLE (63629-6994-2) | 28 tablet | 2016-04-29 | 0000-00-00 | No | No | Current |