Enalapril Maleate
- Product NDC
- 71335-9649
- 11-digit product format
- 713359649
- Labeler code
- 71335
- Product ID
- 71335-9649_52c4701e-6ade-4dbc-82a4-eedf6d9bfaed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075657
- Marketing category
- ANDA
- Marketing start
- 2001-01-23
- Substance
- ENALAPRIL MALEATE
- Active strength
- 20 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 |
|---|
| 71335-9649-1 | 71335964901 | 100 TABLET in 1 BOTTLE (71335-9649-1) | 100 tablet | 2024-04-03 | No | No | Historical |
| 71335-9649-2 | 71335964902 | 60 TABLET in 1 BOTTLE (71335-9649-2) | 60 tablet | 2024-04-03 | No | No | Historical |
| 71335-9649-3 | 71335964903 | 30 TABLET in 1 BOTTLE (71335-9649-3) | 30 tablet | 2023-03-24 | No | No | Historical |
| 71335-9649-4 | 71335964904 | 90 TABLET in 1 BOTTLE (71335-9649-4) | 90 tablet | 2023-02-13 | No | No | Historical |