Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 50090-3135
- 11-digit product format
- 500903135
- Labeler code
- 50090
- Product ID
- 50090-3135_3bea1260-cda6-46d9-bf95-cffe2befea77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091617
- Marketing category
- ANDA
- Marketing start
- 2016-05-23
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3135-0 | Losartan Potassium and Hydrochlorothiazide | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3135 | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20200121_fa797bec-d7db-4630-b49a-20eb60a84500.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3135-0 | 50090313500 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3135-0) | 2017-09-12 | 0000-00-00 | No | No | Current |