Finasteride marketed by Proficient Rx LP under NDC Code 71205-790-30
NDC Code(s) : 71205-790-30, 71205-790-60, 71205-790-90
Packager : Proficient Rx LP
Category : HUMAN PRESCRIPTION DRUG LABEL
DEA Schedule : none
Marketing Status : New Drug Application
INGREDIENTS AND APPEARANCE
FinasterideFinasteride TABLET, COATED |
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PRINCIPAL DISPLAY PANEL
Finasteride Tablets, USP 1 mg
Warning: Finasteride Tablets, USP 1 mg should not be used by women or children. Women who are or may potentially be pregnant must not use Finasteride Tablets, USP 1 mg. They should also not handle crushed or broken tablets of Finasteride Tablets, USP 1 mg. (See Package Insert.)
Rx only
30 Tablets
![71205-790-30](/xml/196f7d23-ed90-46c2-ae34-615e6ec1650b/image-01.jpg)
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