Details for New Drug Application (NDA): 079019
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The generic ingredient in ATOMOXETINE HYDROCHLORIDE is atomoxetine hydrochloride. There are sixteen drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the atomoxetine hydrochloride profile page.
Summary for 079019
Tradename: | ATOMOXETINE HYDROCHLORIDE |
Applicant: | Glenmark Pharms Ltd |
Ingredient: | atomoxetine hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 079019
Mechanism of Action | Norepinephrine Uptake Inhibitors |
Medical Subject Heading (MeSH) Categories for 079019
Suppliers and Packaging for NDA: 079019
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ATOMOXETINE HYDROCHLORIDE | atomoxetine hydrochloride | CAPSULE;ORAL | 079019 | ANDA | Northstar Rx LLC | 16714-755 | 16714-755-01 | 30 CAPSULE in 1 BOTTLE (16714-755-01) |
ATOMOXETINE HYDROCHLORIDE | atomoxetine hydrochloride | CAPSULE;ORAL | 079019 | ANDA | Northstar Rx LLC | 16714-756 | 16714-756-01 | 30 CAPSULE in 1 BOTTLE (16714-756-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 10MG BASE | ||||
Approval Date: | May 30, 2017 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 18MG BASE | ||||
Approval Date: | May 30, 2017 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 25MG BASE | ||||
Approval Date: | May 30, 2017 | TE: | AB | RLD: | No |
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