Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 50090-5937
- 11-digit product format
- 500905937
- Labeler code
- 50090
- Product ID
- 50090-5937_b80bb360-f3d8-44b3-80bd-883b0c49010e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA201845
- Marketing category
- ANDA
- Marketing start
- 2012-10-30
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5937 | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC | 20230901_9045fd7b-5e0b-42ae-874f-9568a8953d4e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5937-0 | 50090593700 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-5937-0) | 2022-03-07 | 0000-00-00 | No | No | Current |
| 50090-5937-1 | 50090593701 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-5937-1) | 2022-03-07 | 0000-00-00 | No | No | Current |