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Dutasteride - Medication Information

Product NDC Code 70771-1347
Drug Name

Dutasteride

Type Generic
Pharm Class 5-alpha Reductase Inhibitor [EPC],
5-alpha Reductase Inhibitors [MoA]
Active Ingredients
Dutasteride .5 mg/1
Route ORAL
Dosage Form CAPSULE, LIQUID FILLED
RxCUI drug identifier 351172
Application Number ANDA204373
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1347-3 30 capsule, liquid filled in 1 bottle (70771-1347-3)
70771-1347-9 90 capsule, liquid filled in 1 bottle (70771-1347-9)
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Spl product data elements

Usually a list of ingredients in a drug product.
Dutasteride Dutasteride DUTASTERIDE DUTASTERIDE BUTYLATED HYDROXYTOLUENE GELATIN GLYCERIN METHYLPARABEN PROPYLPARABEN TITANIUM DIOXIDE ALCOHOL FERROSOFERRIC OXIDE ISOPROPYL ALCOHOL POLYETHYLENE GLYCOL, UNSPECIFIED POLYVINYL ACETATE PHTHALATE PROPYLENE GLYCOL CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES AMMONIA WATER OPAQUE-WHITE Oblong Shaped 641

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1347-3 in bottle of 30 capsules Dutasteride Capsules, 0.5 mg R x only 30 Capsules container label

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API