50090-3135 : Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	50090-3135
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Losartan Potassium and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA091617
Rev. Date:	May 23, 2016

Appearance:

Markings:	L146
Shapes:	Tear
Colors:	Yellow
Size (mm):	11
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

50090-3135-0: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑3135‑0)

Active Ingredients:

Losartan Potassium
Hydrochlorothiazide

Dosage Strength:

50 mg
12.5 mg

Inactive Ingredients:

Microcrystalline Cellulose
Lactose Monohydrate
Starch, Corn
Magnesium Stearate
Hydroxypropyl Cellulose (1600000 Wamw)
Hypromellose, Unspecified
Titanium Dioxide
D&c Yellow No. 10 /

Pharmaceutical Classes:

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

NDC QR Code

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NDC 50090-3135 QR Code

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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.