Details for New Drug Application (NDA): 071655
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The generic ingredient in OXYBUTYNIN CHLORIDE is oxybutynin chloride. There are sixteen drug master file entries for this compound. Forty suppliers are listed for this compound. Additional details are available on the oxybutynin chloride profile page.
Summary for 071655
Tradename: | OXYBUTYNIN CHLORIDE |
Applicant: | Teva Pharms Usa |
Ingredient: | oxybutynin chloride |
Patents: | 0 |
Pharmacology for NDA: 071655
Mechanism of Action | Cholinergic Muscarinic Antagonists |
Suppliers and Packaging for NDA: 071655
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
OXYBUTYNIN CHLORIDE | oxybutynin chloride | TABLET;ORAL | 071655 | ANDA | A-S Medication Solutions | 50090-0318 | 50090-0318-0 | 30 TABLET in 1 BOTTLE (50090-0318-0) |
OXYBUTYNIN CHLORIDE | oxybutynin chloride | TABLET;ORAL | 071655 | ANDA | A-S Medication Solutions | 50090-0318 | 50090-0318-1 | 100 TABLET in 1 BOTTLE (50090-0318-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Nov 14, 1988 | TE: | AB | RLD: | No |
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