Enalapril Maleate
- Product NDC
- 67046-159
- 11-digit product format
- 670460159
- Labeler code
- 67046
- Product ID
- 67046-159_3980589d-98fd-4bf4-9e99-1084bcfd5946
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA075480
- Marketing category
- ANDA
- Marketing start
- 2010-06-28
- Marketing end
- 0000-00-00
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record