Enalapril Maleate
- Product NDC
- 70518-0623
- 11-digit product format
- 705180623
- Labeler code
- 70518
- Product ID
- 70518-0623_6bed433b-7f87-0d4b-e053-2a91aa0a511f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075480
- Marketing category
- ANDA
- Marketing start
- 2017-07-18
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record