Losartan Potassium and Hydrochlorothiazide 12.5 mg / 1; 100 mg / 1 Tablet 30 Tablet, Film Coated
Comprehensive product details for sourcing and verification.
| NDC 11 | 00093-7369-56 |
|---|---|
| Product NDC | 00093-7369 |
| Generic Drug Name | Losartan Potassium and Hydrochlorothiazide |
| Brand Name | Losartan Potassium and Hydrochlorothiazide |
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
| Strength | 12.5 mg / 1; 100 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Tablet, Film Coated |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7369-56) |
| Active Ingredients | Hydrochlorothiazide; Losartan Potassium |
| Marketing Category | ANDA |
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NDC snapshot
Losartan Potassium and Hydrochlorothiazide 12.5 mg / 1; 100 mg / 1 Tablet is tracked under NDC 00093-7369-56 and rolls up into product family 00093-7369. Use this page to confirm the exact presentation before moving into related family or manufacturer pathways.
- Package configuration: 30 Tablet, Film Coated.
- Manufacturer: Teva Pharmaceuticals USA, Inc..
- Dosage form: Tablet.
- Family size: 3 active presentations.
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Official references
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Alternate presentations in this family
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Drug Shortage Information
Public sources include official FDA recall and recall-index pages showing losartan/hydrochlorothiazide shortage-related disruption at the product-family level, plus the Teva product page for exact NDC identification.
Drug Shortage Index family
View Losartan potassium and hydrochlorothiazide in the Drug Shortage IndexCompare related exact NDC products and family-level shortage context for Losartan potassium and hydrochlorothiazide.This section is intended to help healthcare teams review public shortage history and related availability references for this product. Supply conditions can change quickly across manufacturers, distributors, and care settings, and these references may not reflect the latest market status. Premium Rx National does not guarantee completeness or suitability for clinical, operational, or purchasing decisions. Please confirm current availability with FDA, manufacturers, and other authoritative sources before relying on this information.
Losartan Potassium and Hydrochlorothiazide 12.5 mg / 1; 100 mg / 1 Tablet 30 Tablet, Film Coated, NDC 00093-7369-56, is a Teva Pharmaceuticals USA, Inc. 12.5 mg / 1; 100 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated. Current public shortage information is available for this exact presentation.
NDC search formats
- Canonical NDC 11: 00093-7369-56.
- Digits-only NDC 11: 00093736956.
- Possible 10-digit display format: 0093-7369-56 (0093736956).
Helpful product links
- Search by brand name: Losartan Potassium and Hydrochlorothiazide.
- Exact NDC 11: 00093-7369-56.
- Product family NDC: 00093-7369.
- Other package sizes in this family: 1000 Tablet, Film Coated, 90 Tablet, Film Coated.
- Compare related presentations: Losartan Potassium and Hydrochlorothiazide 12.5 mg / 1; 100 mg / 1 Tablet 1000 Tablet, Film Coated, Losartan Potassium and Hydrochlorothiazide 12.5 mg / 1; 100 mg / 1 Tablet 90 Tablet, Film Coated.
Related shortage research
If your team is researching the broader shortage picture, the family page groups related exact NDC items, brand variations, and family-level shortage context in one place.