Details for New Drug Application (NDA): 075049
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The generic ingredient in FLUOXETINE HYDROCHLORIDE is fluoxetine hydrochloride. There are twenty-seven drug master file entries for this compound. Sixty-seven suppliers are listed for this compound. Additional details are available on the fluoxetine hydrochloride profile page.
Summary for 075049
| Tradename: | FLUOXETINE HYDROCHLORIDE |
| Applicant: | Apnar Pharma Lp |
| Ingredient: | fluoxetine hydrochloride |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 075049
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 10MG BASE | ||||
| Approval Date: | Aug 2, 2001 | TE: | AB1 | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 20MG BASE | ||||
| Approval Date: | Jan 29, 2002 | TE: | AB1 | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 40MG BASE | ||||
| Approval Date: | Jan 29, 2002 | TE: | AB | RLD: | No | ||||
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