Enalapril Maleate
- Product NDC
- 68071-3820
- 11-digit product format
- 680713820
- Labeler code
- 68071
- Product ID
- 68071-3820_4cd857af-6c40-c49f-e063-6294a90aa0a1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA213273
- Marketing category
- ANDA
- Marketing start
- 2022-04-24
- 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
- 2027-12-31
- 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 |
|---|
| 68071-3820-3 | 68071382003 | 30 TABLET in 1 BOTTLE (68071-3820-3) | 30 tablet | 2025-03-27 | No | No | Historical |
| 68071-3820-9 | 68071382009 | 90 TABLET in 1 BOTTLE (68071-3820-9) | 90 tablet | 2026-03-12 | No | No | Historical |