Enalapril Maleate
- Product NDC
- 70518-4011
- 11-digit product format
- 705184011
- Labeler code
- 70518
- Product ID
- 70518-4011_43df1c31-c8ac-2fa8-e063-6394a90abf79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA213273
- Marketing category
- ANDA
- Marketing start
- 2024-02-06
- 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 |
|---|
| 70518-4011-1 | 70518401101 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-4011-1) | 90 tablet | 2025-09-13 | No | No | Historical |