50090-3053 : Olmesartan Medoxomil and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	50090-3053
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Olmesartan Medoxomil and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA200532
Rev. Date:	Apr 24, 2017

Appearance:

Markings:	TEVA;7615
Shapes:	Round
Colors:	White
Size (mm):	8
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:

50090-3053-1: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑3053‑1)

Active Ingredients:

Olmesartan Medoxomil
Hydrochlorothiazide

Dosage Strength:

20 mg
12.5 mg

Inactive Ingredients:

Hydroxypropyl Cellulose (200000 Mw)
Ferrosoferric Oxide
Ferric Oxide Red
Ferric Oxide Yellow
Lactose Monohydrate
Low-substituted Hydroxypropyl Cellulose (11% Hydroxypropyl
120000 Mw)
Low-substituted Hydroxypropyl Cellulose (11% Hydroxypropyl
130000 Mw)
Magnesium Stearate
Microcrystalline Cellulose
Polyethylene Glycol 3350
Polyethylene Glycol 4000
Polyvinyl Alcohol, Unspecified
Sodium Lauryl Sulfate
Talc
Titanium Dioxide /

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 50090-3053 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.