Fosinopril Sodium
- Product NDC
- 63629-7663
- 11-digit product format
- 636297663
- Labeler code
- 63629
- Product ID
- 63629-7663_d4a7b10f-a706-42cf-ad1c-499e755aace9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077222
- Marketing category
- ANDA
- Marketing start
- 2016-06-16
- Marketing end
- 0000-00-00
- Substance
- FOSINOPRIL SODIUM
- Active strength
- 10 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 |
|---|
| 63629-7663-1 | 63629766301 | 30 TABLET in 1 BOTTLE (63629-7663-1) | 30 tablet | 2016-06-16 | 0000-00-00 | No | No | Current |
| 63629-7663-2 | 63629766302 | 45 TABLET in 1 BOTTLE (63629-7663-2) | 45 tablet | 2016-06-16 | 0000-00-00 | No | No | Current |
| 63629-7663-3 | 63629766303 | 60 TABLET in 1 BOTTLE (63629-7663-3) | 60 tablet | 2016-06-16 | 0000-00-00 | No | No | Current |
| 63629-7663-4 | 63629766304 | 90 TABLET in 1 BOTTLE (63629-7663-4) | 90 tablet | 2016-06-16 | 0000-00-00 | No | No | Current |
| 63629-7663-5 | 63629766305 | 300 TABLET in 1 BOTTLE (63629-7663-5) | 300 tablet | 2016-06-16 | 0000-00-00 | No | No | Current |
| 63629-7663-6 | 63629766306 | 800 TABLET in 1 BOTTLE (63629-7663-6) | 800 tablet | 2016-06-16 | 0000-00-00 | No | No | Current |
| 63629-7663-7 | 63629766307 | 1000 TABLET in 1 BOTTLE (63629-7663-7) | 1000 tablet | 2016-06-16 | 0000-00-00 | No | No | Current |