Enalapril Maleate
- Product NDC
- 51079-951
- 11-digit product format
- 510790951
- Labeler code
- 51079
- Product ID
- 51079-951_7df4ab0a-daf8-8291-e053-2991aa0a3043
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA075480
- Marketing category
- ANDA
- Marketing start
- 2000-11-15
- Marketing end
- 2019-04-30
- Substance
- ENALAPRIL MALEATE
- Active strength
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record