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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LABELER - Proficient Rx LP(079196022) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
Proficient Rx LP | 079196022 | REPACK(71205-790), RELABEL(71205-790) |
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