ENALAPRIL MALEATE
- Product NDC
- 50090-0692
- 11-digit product format
- 500900692
- Labeler code
- 50090
- Product ID
- 50090-0692_514fcebc-85ba-48fb-9051-48bc05900270
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ENALAPRIL MALEATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075483
- Marketing category
- ANDA
- Marketing start
- 2009-12-11
- 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 |
|---|
| 50090-0692-0 | 50090069200 | 30 TABLET in 1 BOTTLE (50090-0692-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0692-1 | 50090069201 | 60 TABLET in 1 BOTTLE (50090-0692-1) | 60 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0692-3 | 50090069203 | 90 TABLET in 1 BOTTLE (50090-0692-3) | 90 tablet | 2018-12-10 | 0000-00-00 | No | No | Current |