HYZAAR
- Product NDC
- 63629-3183
- 11-digit product format
- 636293183
- Labeler code
- 63629
- Product ID
- 63629-3183_bacd7281-d4fa-4d43-a6cb-d830a664598e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020387
- Marketing category
- NDA
- Marketing start
- 1995-04-28
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
- Active strength
- 50 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-3183-1 | 63629318301 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-3183-1) | 2006-06-13 | 0000-00-00 | No | No | Current |