Details for New Drug Application (NDA): 211051
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The generic ingredient in FLUOXETINE HYDROCHLORIDE is fluoxetine hydrochloride. There are twenty-seven drug master file entries for this compound. Seventy suppliers are listed for this compound. Additional details are available on the fluoxetine hydrochloride profile page.
Summary for 211051
Tradename: | FLUOXETINE HYDROCHLORIDE |
Applicant: | Teva Pharms Usa |
Ingredient: | fluoxetine hydrochloride |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 211051
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | EQ 60MG BASE | ||||
Approval Date: | Dec 3, 2018 | TE: | RLD: | No |
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