Details for New Drug Application (NDA): 075388
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The generic ingredient in BUSPIRONE HYDROCHLORIDE is buspirone hydrochloride. There are nineteen drug master file entries for this compound. Forty suppliers are listed for this compound. Additional details are available on the buspirone hydrochloride profile page.
Summary for 075388
Tradename: | BUSPIRONE HYDROCHLORIDE |
Applicant: | Oxford Pharms |
Ingredient: | buspirone hydrochloride |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Medical Subject Heading (MeSH) Categories for 075388
Suppliers and Packaging for NDA: 075388
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
BUSPIRONE HYDROCHLORIDE | buspirone hydrochloride | TABLET;ORAL | 075388 | ANDA | A-S Medication Solutions | 50090-6649 | 50090-6649-0 | 30 TABLET in 1 BOTTLE (50090-6649-0) |
BUSPIRONE HYDROCHLORIDE | buspirone hydrochloride | TABLET;ORAL | 075388 | ANDA | A-S Medication Solutions | 50090-6649 | 50090-6649-1 | 90 TABLET in 1 BOTTLE (50090-6649-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | May 9, 2002 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | May 9, 2002 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 15MG | ||||
Approval Date: | May 9, 2002 | TE: | AB | RLD: | No |
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