Enalapril Maleate
- Product NDC
- 71335-2252
- 11-digit product format
- 713352252
- Labeler code
- 71335
- Product ID
- 71335-2252_d7710f3a-7f24-4881-9eb1-779058f0ee10
- 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
- 2.5 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 |
|---|
| 71335-2252-1 | 71335225201 | 30 TABLET in 1 BOTTLE (71335-2252-1) | 30 tablet | 2023-10-02 | No | No | Historical |
| 71335-2252-2 | 71335225202 | 90 TABLET in 1 BOTTLE (71335-2252-2) | 90 tablet | 2023-10-02 | No | No | Historical |