Enalapril Maleate
- Product NDC
- 51672-4245
- 11-digit product format
- 516724245
- Labeler code
- 51672
- Product ID
- 51672-4245_e64450c0-8dde-4920-9bf9-c714e09e1566
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- ANDA075657
- Marketing category
- ANDA
- Marketing start
- 2001-01-23
- Substance
- ENALAPRIL MALEATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9O25354EPJ | ENALAPRIL MALEATE | 76095-16-4 | ENALAPRIL MALEATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51672-4245-1 | 51672424501 | 100 TABLET in 1 BOTTLE (51672-4245-1) | 100 tablet | 2023-07-17 | No | No | Historical |
| 51672-4245-3 | 51672424503 | 1000 TABLET in 1 BOTTLE (51672-4245-3) | 1000 tablet | 2023-07-17 | No | No | Historical |