Captopril
- Product NDC
- 63629-8729
- 11-digit product format
- 636298729
- Labeler code
- 63629
- Product ID
- 63629-8729_35e62e03-4ca6-400e-adfd-28e8b641ea3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074477
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- Substance
- CAPTOPRIL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9G64RSX1XD | CAPTOPRIL | 62571-86-2 | CAPTOPRIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-8729-1 | 63629872901 | 100 TABLET in 1 BOTTLE (63629-8729-1) | 100 tablet | 2021-08-19 | No | No | Historical |