50090-5295 : Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	50090-5295
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Losartan Potassium and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA077157
Rev. Date:	Apr 6, 2010

NDC Package Codes:

50090-5295-0: 30 TABLET, FILM COATED IN 1 BOTTLE (50090‑5295‑0)
50090-5295-1: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑5295‑1)

Active Ingredients:

Losartan Potassium
Hydrochlorothiazide

Dosage Strength:

100 mg
12.5 mg

Pharmaceutical Classes:

Angiotensin 2 Receptor Antagonists [MoA]
Angiotensin 2 Receptor Blocker [EPC]
Increased Diuresis [PE]
Thiazide Diuretic [EPC]
Thiazides [CS]

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.