Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 71335-1025
- 11-digit product format
- 713351025
- Labeler code
- 71335
- Product ID
- 71335-1025_633099a8-68d0-4535-bc3f-d6f643a21e1c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091617
- Marketing category
- ANDA
- Marketing start
- 2016-05-23
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
- Active strength
- 25 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1025-1 | 71335102501 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1025-1) | 2018-12-14 | 0000-00-00 | No | No | Current |
| 71335-1025-2 | 71335102502 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1025-2) | 2018-12-14 | 0000-00-00 | No | No | Current |
| 71335-1025-3 | 71335102503 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1025-3) | 2018-12-14 | 0000-00-00 | No | No | Current |