ENALAPRIL MALEATE
- Product NDC
- 35356-869
- 11-digit product format
- 353560869
- Labeler code
- 35356
- Product ID
- 35356-869_cdbbe11e-c763-4891-ab70-6c0d6fad84f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ENALAPRIL MALEATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA075483
- Marketing category
- ANDA
- Marketing start
- 2009-12-11
- 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