71335-0181 : Losartan Potassium 50 mg Oral Tablet

NDC:	71335-0181
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Losartan Potassium
Dosage Form:	Oral Tablet
Application #:	ANDA090467
Rev. Date:	Oct 6, 2010

Appearance:

Markings:	114
Shapes:	Oval
Colors:	White
Size (mm):	10
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:

71335-0181-1: 30 TABLET IN 1 BOTTLE (71335‑0181‑1)
71335-0181-2: 90 TABLET IN 1 BOTTLE (71335‑0181‑2)
71335-0181-3: 60 TABLET IN 1 BOTTLE (71335‑0181‑3)
71335-0181-4: 120 TABLET IN 1 BOTTLE (71335‑0181‑4)
71335-0181-5: 100 TABLET IN 1 BOTTLE (71335‑0181‑5)
71335-0181-6: 180 TABLET IN 1 BOTTLE (71335‑0181‑6)
71335-0181-7: 10 TABLET IN 1 BOTTLE (71335‑0181‑7)

Active Ingredients:

Losartan Potassium

Dosage Strength:

50 mg

Inactive Ingredients:

Microcrystalline Cellulose
Hydroxypropyl Cellulose (1200000 Mw)
Hypromellose 2910 (6 Mpa.s)
Anhydrous Lactose
Magnesium Stearate
Starch, Corn
Talc
Titanium Dioxide
Silicon Dioxide

Pharmaceutical Classes:

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

NDC QR Code

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NDC 71335-0181 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.