Enalapril Maleate
- Product NDC
- 70518-0520
- 11-digit product format
- 705180520
- Labeler code
- 70518
- Product ID
- 70518-0520_a4f2dcca-ab3d-7006-e053-2995a90a27d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-05-10
- Marketing end
- 0000-00-00
- Substance
- ENALAPRIL MALEATE
- Active strength
- 3 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-0520-0 | 70518052000 | 30 TABLET in 1 BLISTER PACK (70518-0520-0) | 30 tablet | 2017-05-10 | 0000-00-00 | No | No | Current |
| 70518-0520-1 | 70518052001 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0520-1) | 90 tablet | 2017-11-29 | 0000-00-00 | No | No | Current |