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FDA Drug information

Losartan Potassium

Read time: 1 mins
Marketing start date: 23 Dec 2024
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Summary of product characteristics


Effective Time

20221018

Version

10

Spl Product Data Elements

Losartan Potassium Losartan Potassium LOSARTAN POTASSIUM LOSARTAN HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO TALC TITANIUM DIOXIDE SILICON DIOXIDE CELLULOSE, MICROCRYSTALLINE HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED STARCH, CORN POLYETHYLENE GLYCOL, UNSPECIFIED WHITE TO OFF-WHITE CAPSULE Z;2 Losartan Potassium Losartan Potassium LOSARTAN POTASSIUM LOSARTAN HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO TALC TITANIUM DIOXIDE SILICON DIOXIDE CELLULOSE, MICROCRYSTALLINE HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED STARCH, CORN POLYETHYLENE GLYCOL, UNSPECIFIED WHITE TO OFF-WHITE CAPSULE Z16 Losartan Potassium Losartan Potassium LOSARTAN POTASSIUM LOSARTAN HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO TALC TITANIUM DIOXIDE SILICON DIOXIDE CELLULOSE, MICROCRYSTALLINE HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED STARCH, CORN POLYETHYLENE GLYCOL, UNSPECIFIED WHITE TO OFF-WHITE CAPSULE Z18

Application Number

ANDA078243

Brand Name

Losartan Potassium

Generic Name

Losartan Potassium

Product Ndc

65841-729

Product Type

HUMAN PRESCRIPTION DRUG

Route

ORAL

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 65841-729-01 Losartan Potassium Tablets USP, 25 mg Rx Only 100 Tablets Zydus NDC 65841-730-01 Losartan Potassium Tablets USP, 50 mg Rx Only 100 Tablets Zydus NDC 65841-731-01 Losartan Potassium Tablets USP, 100 mg Rx Only 100 Tablets Zydus 25 mg 50 mg 100 mg

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