50090-3701 : Olmesartan Medoxomil and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	50090-3701
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Olmesartan Medoxomil and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA205391
Rev. Date:	Apr 24, 2017

Appearance:

Markings:	K;23
Shapes:	Round
Colors:	Yellow
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:

50090-3701-0: 30 TABLET, FILM COATED IN 1 BOTTLE (50090‑3701‑0)
50090-3701-1: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑3701‑1)

Active Ingredients:

Olmesartan Medoxomil
Hydrochlorothiazide

Dosage Strength:

20 mg
12.5 mg

Inactive Ingredients:

Hydroxypropyl Cellulose (110000 Wamw)
Hypromellose 2910 (3 Mpa.s)
Ferric Oxide Red
Ferric Oxide Yellow
Lactose Monohydrate
Low-substituted Hydroxypropyl Cellulose, Unspecified
Magnesium Stearate
Microcrystalline Cellulose
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 50090-3701 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.