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| Product NDC Code | 70771-1152 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Finasteride |
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| Type | Generic | ||||||||||
| Pharm Class | 5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA] |
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| Active Ingredients |
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| Route | ORAL | ||||||||||
| Dosage Form | TABLET, FILM COATED | ||||||||||
| RxCUI drug identifier | 310346 | ||||||||||
| Application Number | ANDA078900 | ||||||||||
| Labeler Name | Zydus Lifesciences Limited | ||||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Spl product data elements
Usually a list of ingredients in a drug product.Finasteride Finasteride FINASTERIDE FINASTERIDE DOCUSATE SODIUM FD&C BLUE NO. 2 HYDROXYPROPYL CELLULOSE (1600000 WAMW) FERRIC OXIDE YELLOW LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE STARCH, CORN SODIUM STARCH GLYCOLATE TYPE A POTATO TALC TITANIUM DIOXIDE SHELLAC FERROSOFERRIC OXIDE HYPROMELLOSES blue ROUND ZE;56
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 70771-1152-0 in bottle of 1000 tablets Finasteride Tablets USP, 5 mg R x only 1000 tablets Finasteride Tablets, 5 mg
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