Captopril
- Product NDC
- 51079-864
- 11-digit product format
- 510790864
- Labeler code
- 51079
- Product ID
- 51079-864_7baaae0c-cadb-7516-e053-2991aa0afe71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA074434
- Marketing category
- ANDA
- Marketing start
- 1996-02-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51079-864-20 | 51079086420 | 100 BLISTER PACK in 1 CARTON (51079-864-20) > 1 TABLET in 1 BLISTER PACK (51079-864-01) | 100 blister pack | 1996-02-14 | 0000-00-00 | No | No | Current |