63629-6845 : Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated

NDC:	63629-6845
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Losartan Potassium and Hydrochlorothiazide
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA091629
Rev. Date:	Oct 6, 2010

Appearance:

Markings:	E;49
Shapes:	Oval
Colors:	Yellow
Size (mm):	17
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.

E 49: (16714-225) Losartan Potassium and Hydrochlorothiazide Oral Tablet, Film Coated by Bryant Ranch Prepack

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

63629-6845-1: 30 TABLET, FILM COATED IN 1 BOTTLE (63629‑6845‑1)

Active Ingredients:

Losartan Potassium
Hydrochlorothiazide

Dosage Strength:

100 mg
25 mg

Inactive Ingredients:

Silicon Dioxide
Hydroxypropyl Cellulose (1200000 Mw)
Hypromellose 2910 (6 Mpa.s)
Lactose Monohydrate
Magnesium Stearate
Microcrystalline Cellulose
Starch, Corn
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 63629-6845 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.