Enalapril Maleate
- Product NDC
- 70518-1821
- 11-digit product format
- 705181821
- Labeler code
- 70518
- Product ID
- 70518-1821_8401cc5f-282b-79df-e053-2a91aa0af04d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-01-24
- Marketing end
- 0000-00-00
- Substance
- ENALAPRIL MALEATE
- Active strength
- 3 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