Enalapril Maleate
- Product NDC
- 68788-7309
- 11-digit product format
- 687887309
- Labeler code
- 68788
- Product ID
- 68788-7309_112ae2b7-6d20-4d53-9f28-8a6721d90240
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- NDA018998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-01-04
- 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 |
|---|
| 68788-7309-3 | 68788730903 | 30 TABLET in 1 BOTTLE (68788-7309-3) | 30 tablet | 2019-01-04 | 0000-00-00 | No | No | Current |
| 68788-7309-6 | 68788730906 | 60 TABLET in 1 BOTTLE (68788-7309-6) | 60 tablet | 2019-01-04 | 0000-00-00 | No | No | Current |
| 68788-7309-9 | 68788730909 | 90 TABLET in 1 BOTTLE (68788-7309-9) | 90 tablet | 2019-01-04 | 0000-00-00 | No | No | Current |