Losartan Potassium and Hydrochlorothiazide 12.5 mg / 1; 100 mg / 1 Tablet 30 Tablet, Film Coated
Reference details for licensed healthcare facility review 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 review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 30 Tablet, Film Coated.
- Manufacturer: Teva Pharmaceuticals USA, Inc..
- Dosage form: Tablet.
- Family size: 3 indexed presentations.
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Official references
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Alternate presentations in this family
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Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 20 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
View Potential Alternative Hublosartan potassium and hydrochlorothiazide 12.5 mg / 1; 100 mg / 1 Tablet 30 Tablet, Film Coated Bottle20 package-level listings in the comparison hub.Sample package-level pages in this comparison set
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 NDC identification.
Drug Shortage Index family
View Losartan potassium and hydrochlorothiazide in the Drug Shortage IndexCompare related NDC-level product references 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 product reference.
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
- 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
- VA classification code: CV400
- VA classification code description: ANTIHYPERTENSIVE COMBINATIONS
- CMOP ID: H0481
- VUID: 4025049