Details for New Drug Application (NDA): 075464
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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-one suppliers are listed for this compound. Additional details are available on the fluoxetine hydrochloride profile page.
Summary for 075464
Tradename: | FLUOXETINE HYDROCHLORIDE |
Applicant: | Landela Pharm |
Ingredient: | fluoxetine hydrochloride |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 075464
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 10MG BASE | ||||
Approval Date: | Jan 30, 2002 | TE: | AB1 | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 20MG BASE | ||||
Approval Date: | Jan 30, 2002 | TE: | AB1 | RLD: | No |
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