Enalapril Maleate
- Product NDC
- 70934-702
- 11-digit product format
- 709340702
- Labeler code
- 70934
- Product ID
- 70934-702_b86ae33a-092f-2eb9-e053-2a95a90a1dce
- 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
- 2021-01-04
- 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
- 2022-12-31
- 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 |
|---|
| 70934-702-30 | 70934070230 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-702-30) | 30 tablet | 2021-01-04 | 0000-00-00 | No | No | Current |