Captopril
- Product NDC
- 50090-4296
- 11-digit product format
- 500904296
- Labeler code
- 50090
- Product ID
- 50090-4296_ff2ad92e-13f7-4943-96ab-0d3934e8c65d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074477
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- Marketing end
- 0000-00-00
- Substance
- CAPTOPRIL
- Active strength
- 25 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4296-3 | 50090429603 | 60 TABLET in 1 BOTTLE (50090-4296-3) | 60 tablet | 2019-05-13 | 0000-00-00 | No | No | Current |