Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 68788-7758
- 11-digit product format
- 687887758
- Labeler code
- 68788
- Product ID
- 68788-7758_0b51f43c-7287-4932-80d4-eb6ad4f540fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078245
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
- Active strength
- 13 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7758-1 | 68788775801 | 100 TABLET in 1 BOTTLE (68788-7758-1) | 100 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7758-3 | 68788775803 | 30 TABLET in 1 BOTTLE (68788-7758-3) | 30 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7758-6 | 68788775806 | 60 TABLET in 1 BOTTLE (68788-7758-6) | 60 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7758-9 | 68788775809 | 90 TABLET in 1 BOTTLE (68788-7758-9) | 90 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |