71335-0262 : Losartan Potassium 50 mg Oral Tablet, Film Coated

NDC:	71335-0262
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Losartan Potassium
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA091497
Rev. Date:	Jul 30, 2014

Appearance:

Markings:	S;112
Shapes:	Round
Colors:	White
Size (mm):	8
Segments: ^*	2
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

71335-0262-1: 30 TABLET, FILM COATED IN 1 BOTTLE (71335‑0262‑1)
71335-0262-2: 90 TABLET, FILM COATED IN 1 BOTTLE (71335‑0262‑2)
71335-0262-3: 60 TABLET, FILM COATED IN 1 BOTTLE (71335‑0262‑3)
71335-0262-4: 120 TABLET, FILM COATED IN 1 BOTTLE (71335‑0262‑4)
71335-0262-5: 100 TABLET, FILM COATED IN 1 BOTTLE (71335‑0262‑5)
71335-0262-6: 180 TABLET, FILM COATED IN 1 BOTTLE (71335‑0262‑6)
71335-0262-7: 10 TABLET, FILM COATED IN 1 BOTTLE (71335‑0262‑7)

Active Ingredients:

Losartan Potassium

Dosage Strength:

50 mg

Inactive Ingredients:

Microcrystalline Cellulose
Lactose Monohydrate
Starch, Corn
Magnesium Stearate
Hydroxypropyl Cellulose (1200000 Mw)
Hypromellose, Unspecified
Titanium Dioxide

Pharmaceutical Classes:

Angiotensin 2 Receptor Antagonists [MoA]
Angiotensin 2 Receptor Blocker [EPC]

NDC QR Code

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NDC 71335-0262 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.