CAPTOPRIL
- Product NDC
- 57721-904
- 11-digit product format
- 577210904
- Labeler code
- 57721
- Product ID
- 57721-904_b7be9918-a633-44d4-8965-d19bab8b83dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Windlas Biotech Limited
- Application
- ANDA074532
- Marketing category
- ANDA
- Marketing start
- 1997-03-28
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 57721-904-01 | CAPTOPRIL | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 57721-904-02 | CAPTOPRIL | 1000 in 1 BOTTLE | TABLET | 1000 | | 3 |
| 57721-904-05 | CAPTOPRIL | 5000 in 1 POUCH | TABLET | 5000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 57721-904 | CAPTOPRIL TABLET [WINDLAS BIOTECH LIMITED] | 3 | Legacy NDC, 3 package rows | 20210715_2f87bcd5-6fc8-4084-9644-519fa5ee8a6b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57721-904-01 | 57721090401 | 100 TABLET in 1 BOTTLE (57721-904-01) | 100 tablet | 1997-03-28 | 0000-00-00 | No | No | Current |
| 57721-904-02 | 57721090402 | 1000 TABLET in 1 BOTTLE (57721-904-02) | 1000 tablet | 1997-03-28 | 0000-00-00 | No | No | Current |
| 57721-904-05 | 57721090405 | 5000 TABLET in 1 POUCH (57721-904-05) | 5000 tablet | 1997-03-28 | 0000-00-00 | No | No | Current |