ENALAPRIL MALEATE
- Product NDC
- 0904-5611
- 11-digit product format
- 009045611
- Labeler code
- 0904
- Product ID
- 0904-5611_6002936e-3077-42f4-8e89-81259bbfbfb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ENALAPRIL MALEATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- 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
- 2020-12-31
- 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 |
|---|
| 0904-5611-61 | 00904561161 | 100 BLISTER PACK in 1 CARTON (0904-5611-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2009-12-11 | 0000-00-00 | No | No | Current |