Enalapril Maleate
- Product NDC
- 70518-0045
- 11-digit product format
- 705180045
- Labeler code
- 70518
- Product ID
- 70518-0045_de4998ee-3557-01c6-e053-2a95a90a052a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075657
- Marketing category
- ANDA
- Marketing start
- 2016-12-07
- 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
- 2023-12-31
- 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 |
|---|
| 70518-0045-0 | 70518004500 | 30 TABLET in 1 BLISTER PACK (70518-0045-0) | 30 tablet | 2016-12-07 | 0000-00-00 | No | No | Current |
| 70518-0045-1 | 70518004501 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0045-1) | 90 tablet | 2019-04-10 | 0000-00-00 | No | No | Current |