Details for New Drug Application (NDA): 075292
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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 075292
Tradename: | FLUOXETINE HYDROCHLORIDE |
Applicant: | Nostrum Labs Inc |
Ingredient: | fluoxetine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 075292
Mechanism of Action | Serotonin Uptake Inhibitors |
Medical Subject Heading (MeSH) Categories for 075292
Suppliers and Packaging for NDA: 075292
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
FLUOXETINE HYDROCHLORIDE | fluoxetine hydrochloride | SOLUTION;ORAL | 075292 | ANDA | Nostrum Laboratories Inc. | 29033-503 | 29033-503-31 | 120 mL in 1 BOTTLE, PLASTIC (29033-503-31) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | EQ 20MG BASE/5ML | ||||
Approval Date: | Feb 7, 2002 | TE: | AA | RLD: | No |
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