ENALAPRIL MALEATE
- Product NDC
- 55289-591
- 11-digit product format
- 552890591
- Labeler code
- 55289
- Product ID
- 55289-591_dd044141-3c81-18b1-e053-2995a90a3fc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ENALAPRIL MALEATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075483
- Marketing category
- ANDA
- Marketing start
- 2009-12-11
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-591-30 | 55289059130 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-591-30) | 30 tablet | 2016-02-09 | 0000-00-00 | No | No | Current |
| 55289-591-90 | 55289059190 | 90 TABLET in 1 BOTTLE, PLASTIC (55289-591-90) | 90 tablet | 2016-02-09 | 0000-00-00 | No | No | Current |