ENALAPRIL MALEATE
- Product NDC
- 35356-871
- 11-digit product format
- 353560871
- Labeler code
- 35356
- Product ID
- 35356-871_03c76f92-0331-4c36-b4d9-e53605e3f703
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ENALAPRIL MALEATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- 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
- 2022-12-31
- 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 |
|---|
| 35356-871-90 | 35356087190 | 90 TABLET in 1 BOTTLE (35356-871-90) | 90 tablet | 2009-12-11 | 0000-00-00 | No | No | Current |