ENALAPRIL MALEATE
- Product NDC
- 55289-694
- 11-digit product format
- 552890694
- Labeler code
- 55289
- Product ID
- 55289-694_dd044b83-e2cc-66e8-e053-2a95a90aa3fd
- 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
- 5 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 |
|---|
| 55289-694-10 | 55289069410 | 10 TABLET in 1 BOTTLE, PLASTIC (55289-694-10) | 10 tablet | 2010-07-05 | 0000-00-00 | No | No | Current |
| 55289-694-30 | 55289069430 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-694-30) | 30 tablet | 2010-07-05 | 0000-00-00 | No | No | Current |
| 55289-694-90 | 55289069490 | 90 TABLET in 1 BOTTLE, PLASTIC (55289-694-90) | 90 tablet | 2010-07-05 | 0000-00-00 | No | No | Current |