Enalapril Maleate
- Product NDC
- 70934-492
- 11-digit product format
- 709340492
- Labeler code
- 70934
- Product ID
- 70934-492_a839e6df-7004-8e6a-e053-2995a90a7536
- 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
- 2020-01-09
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-492-30 | 70934049230 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-492-30) | 30 tablet | 2020-01-09 | 0000-00-00 | No | No | Current |
| 70934-492-90 | 70934049290 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-492-90) | 90 tablet | 2020-05-19 | 0000-00-00 | No | No | Current |