Enalapril Maleate
- Product NDC
- 50090-3166
- 11-digit product format
- 500903166
- Labeler code
- 50090
- Product ID
- 50090-3166_afd3dc85-461c-43b1-9d4d-53a9d5daf183
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075479
- Marketing category
- ANDA
- Marketing start
- 2000-08-23
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9O25354EPJ | ENALAPRIL MALEATE | 76095-16-4 | ENALAPRIL MALEATE |