Enalapril Maleate
- Product NDC
- 70518-1351
- 11-digit product format
- 705181351
- Labeler code
- 70518
- Product ID
- 70518-1351_9254e808-faaa-29c1-e053-2a95a90a3782
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075657
- Marketing category
- ANDA
- Marketing start
- 2018-08-07
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record