Enalapril Maleate and Hydrochlorothiazide
- Product NDC
- 71335-0870
- 11-digit product format
- 713350870
- Labeler code
- 71335
- Product ID
- 71335-0870_acc05043-acbd-4b7b-bb4a-8fb9e05cb3ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Enalapril Maleate and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075727
- Marketing category
- ANDA
- Marketing start
- 2016-03-31
- 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
- 2023-12-31
- 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 |
|---|
| 71335-0870-1 | 71335087001 | 30 TABLET in 1 BOTTLE (71335-0870-1) | 30 tablet | 2016-03-31 | 0000-00-00 | No | No | Current |
| 71335-0870-2 | 71335087002 | 100 TABLET in 1 BOTTLE (71335-0870-2) | 100 tablet | 2016-03-31 | 0000-00-00 | No | No | Current |