Enalapril Maleate
- Product NDC
- 68071-3303
- 11-digit product format
- 680713303
- Labeler code
- 68071
- Product ID
- 68071-3303_bb29aa84-4df2-6336-e053-2a95a90afcef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- NDA018998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1985-12-24
- 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
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 |
|---|
| 68071-3303-1 | 68071330301 | 120 TABLET in 1 BOTTLE (68071-3303-1) | 120 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |
| 68071-3303-3 | 68071330303 | 30 TABLET in 1 BOTTLE (68071-3303-3) | 30 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |
| 68071-3303-6 | 68071330306 | 60 TABLET in 1 BOTTLE (68071-3303-6) | 60 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |
| 68071-3303-9 | 68071330309 | 90 TABLET in 1 BOTTLE (68071-3303-9) | 90 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |