Enalapril Maleate
- Product NDC
- 68071-3173
- 11-digit product format
- 680713173
- Labeler code
- 68071
- Product ID
- 68071-3173_bb13ca9a-4430-8fb4-e053-2a95a90a1b5a
- 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
- 1988-07-26
- 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 |
|---|
| 68071-3173-3 | 68071317303 | 30 TABLET in 1 BOTTLE (68071-3173-3) | 30 tablet | 2017-03-17 | 0000-00-00 | No | No | Current |
| 68071-3173-9 | 68071317309 | 90 TABLET in 1 BOTTLE (68071-3173-9) | 90 tablet | 2017-03-17 | 0000-00-00 | No | No | Current |