Captopril
- Product NDC
- 71335-2358
- 11-digit product format
- 713352358
- Labeler code
- 71335
- Product ID
- 71335-2358_6eacdc8f-6864-4f91-aa3c-54b55366c76c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212809
- Marketing category
- ANDA
- Marketing start
- 2019-12-13
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Captopril
- Listing expiration
- 2027-12-31
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 |
|---|
| 71335-2358-1 | Captopril | 90 in 1 BOTTLE | TABLET | 90 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2358 | CAPTOPRIL TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240229_66604c8e-f6b6-4cf9-9561-f1cb4af0e0d6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2358-1 | 71335235801 | 90 TABLET in 1 BOTTLE (71335-2358-1) | 90 tablet | 2024-02-27 | No | No | Historical |