Enalapril Maleate and Hydrochlorothiazide
- Product NDC
- 68071-4144
- 11-digit product format
- 680714144
- Labeler code
- 68071
- Product ID
- 68071-4144_bb2d055f-25fb-3497-e053-2995a90a4457
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075788
- Marketing category
- ANDA
- Marketing start
- 2001-09-18
- Marketing end
- 0000-00-00
- Substance
- ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- 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 |
|---|
| 68071-4144-3 | 68071414403 | 30 TABLET in 1 BOTTLE (68071-4144-3) | 30 tablet | 2017-11-01 | 0000-00-00 | No | No | Current |
| 68071-4144-6 | 68071414406 | 60 TABLET in 1 BOTTLE (68071-4144-6) | 60 tablet | 2017-11-01 | 0000-00-00 | No | No | Current |
| 68071-4144-9 | 68071414409 | 90 TABLET in 1 BOTTLE (68071-4144-9) | 90 tablet | 2017-11-01 | 0000-00-00 | No | No | Current |