Enalapril Maleate
- Product NDC
- 70518-1190
- 11-digit product format
- 705181190
- Labeler code
- 70518
- Product ID
- 70518-1190_e32459a3-81f0-ea28-e053-2a95a90aa2e5
- 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
- 2018-05-14
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1190-0 | 70518119000 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1190-0) | 90 tablet | 2018-05-14 | 0000-00-00 | No | No | Current |
| 70518-1190-1 | 70518119001 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1190-1) | 90 tablet | 2020-07-23 | 0000-00-00 | No | No | Current |