Enalapril Maleate
- Product NDC
- 70518-1564
- 11-digit product format
- 705181564
- Labeler code
- 70518
- Product ID
- 70518-1564_eff7b5a2-229b-d3b4-e053-2995a90a016e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075657
- Marketing category
- ANDA
- Marketing start
- 2018-10-22
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-1564-0 | 70518156400 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1564-0) | 90 tablet | 2018-10-22 | 0000-00-00 | No | No | Current |
| 70518-1564-1 | 70518156401 | 30 TABLET in 1 BLISTER PACK (70518-1564-1) | 30 tablet | 2018-10-25 | 0000-00-00 | No | No | Current |