Enalapril Maleate
- Product NDC
- 70934-566
- 11-digit product format
- 709340566
- Labeler code
- 70934
- Product ID
- 70934-566_ac0e0d7a-d5cf-7088-e053-2a95a90a04c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA075657
- Marketing category
- ANDA
- Marketing start
- 2020-03-26
- 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
- 2021-12-31
- 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 |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-566-30 | 70934056630 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-566-30) | 30 tablet | 2020-03-26 | 0000-00-00 | No | No | Current |