ENALAPRIL MALEATE
- Product NDC
- 55289-984
- 11-digit product format
- 552890984
- Labeler code
- 55289
- Product ID
- 55289-984_ded2b1d6-d5ac-ae41-e053-2995a90a7bf8
- 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
- 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 |
|---|
| 55289-984-30 | 55289098430 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-984-30) | 30 tablet | 2015-04-21 | 0000-00-00 | No | No | Current |
| 55289-984-90 | 55289098490 | 90 TABLET in 1 BOTTLE, PLASTIC (55289-984-90) | 90 tablet | 2015-04-21 | 0000-00-00 | No | No | Current |