63629-5032 : Hctz 12.5 mg / Losartan Potassium 50 mg Oral Tablet

NDC:	63629-5032
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Losartan Potassium and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA078385
Rev. Date:	Oct 4, 2010

Appearance:

Markings:	ZD18
Shapes:	Capsule
Colors:	White
Size (mm):	12
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:

63629-5032-1: 90 TABLET, FILM COATED IN 1 BOTTLE (63629‑5032‑1)
63629-5032-2: 60 TABLET, FILM COATED IN 1 BOTTLE (63629‑5032‑2)
63629-5032-3: 30 TABLET, FILM COATED IN 1 BOTTLE (63629‑5032‑3)

Active Ingredients:

Hydrochlorothiazide
Losartan Potassium

Dosage Strength:

12.5 mg
50 mg

Inactive Ingredients:

Hypromelloses
Lactose Monohydrate
Magnesium Stearate
Polyethylene Glycols
Sodium Starch Glycolate Type a Potato
Talc
Titanium Dioxide
Silicon Dioxide
Cellulose, Microcrystalline
Hydroxypropyl Cellulose, Low Substituted
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 63629-5032 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.