Enalapril maleate
- Product NDC
- 69043-035
- 11-digit product format
- 690430035
- Labeler code
- 69043
- Product ID
- 69043-035_1532d3be-df01-45bf-8908-a8af87feee3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cronus Pharma LLC
- Application
- ANDA075479
- Marketing category
- ANDA
- Marketing start
- 2021-05-12
- Marketing end
- 0000-00-00
- Substance
- ENALAPRIL MALEATE
- Active strength
- 3 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69043-035-01 | 69043003501 | 100 TABLET in 1 BOTTLE (69043-035-01) | 100 tablet | 2021-05-12 | 0000-00-00 | No | No | Current |
| 69043-035-99 | 69043003599 | 1000 TABLET in 1 BOTTLE (69043-035-99) | 1000 tablet | 2021-05-12 | 0000-00-00 | No | No | Current |