captopril
- Product NDC
- 63629-3554
- 11-digit product format
- 636293554
- Labeler code
- 63629
- Product ID
- 63629-3554_3ebb6074-91f0-4937-a62f-07e5ec5266e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074677
- Marketing category
- ANDA
- Marketing start
- 2019-08-20
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- captopril
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAPTOPRIL | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9G64RSX1XD |
| Rxcui | 308964 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-3554-1 | captopril | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-3554-1 | 63629355401 | 90 TABLET in 1 BOTTLE (63629-3554-1) | 90 tablet | 2025-06-26 | No | No | Current |