50090-1701 : Valsartan and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	50090-1701
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Valsartan and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA078946
Rev. Date:	Mar 21, 2013

Appearance:

Markings:	LU;P11
Shapes:	Capsule
Colors:	Pink
Size (mm):	13
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:

50090-1701-0: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑1701‑0)

Active Ingredients:

Hydrochlorothiazide
Valsartan

Dosage Strength:

12.5 mg
80 mg

Inactive Ingredients:

Croscarmellose Sodium
Ferric Oxide Yellow
Hypromelloses
Silicon Dioxide
Polyethylene Glycol 400
Cellulose, Microcrystalline
Crospovidone
Magnesium Stearate
Titanium Dioxide
Ferric Oxide Red
Starch, Corn

Pharmaceutical Classes:

Increased Diuresis [PE]
Thiazide Diuretic [EPC]
Thiazides [Chemical/Ingredient]
Angiotensin 2 Receptor Antagonists [MoA]
Angiotensin 2 Receptor Blocker [EPC]

NDC QR Code

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NDC 50090-1701 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.