Captopril
- Product NDC
- 0378-3022
- 11-digit product format
- 003783022
- Labeler code
- 0378
- Product ID
- 0378-3022_abb87e44-070a-4c1f-af3e-d5ea259edbc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- captopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA074434
- Marketing category
- ANDA
- Marketing start
- 1996-02-13
- Marketing end
- 0000-00-00
- Substance
- CAPTOPRIL
- Active strength
- 100 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 |
|---|
| 0378-3022-01 | 00378302201 | 100 TABLET in 1 BOTTLE, PLASTIC (0378-3022-01) | 100 tablet | 1996-02-13 | 0000-00-00 | No | No | Current |