Details for New Drug Application (NDA): 071450
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The generic ingredient in ALLOPURINOL is allopurinol sodium. There are twenty-two drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the allopurinol sodium profile page.
Summary for 071450
Tradename: | ALLOPURINOL |
Applicant: | Sun Pharm Industries |
Ingredient: | allopurinol |
Patents: | 0 |
Pharmacology for NDA: 071450
Mechanism of Action | Xanthine Oxidase Inhibitors |
Medical Subject Heading (MeSH) Categories for 071450
Suppliers and Packaging for NDA: 071450
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ALLOPURINOL | allopurinol | TABLET;ORAL | 071450 | ANDA | PD-Rx Pharmaceuticals, Inc. | 43063-934 | 43063-934-01 | 100 TABLET in 1 BOTTLE, PLASTIC (43063-934-01) |
ALLOPURINOL | allopurinol | TABLET;ORAL | 071450 | ANDA | PD-Rx Pharmaceuticals, Inc. | 43063-935 | 43063-935-01 | 100 TABLET in 1 BOTTLE, PLASTIC (43063-935-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 300MG | ||||
Approval Date: | Jan 9, 1987 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 100MG | ||||
Approval Date: | Jan 9, 1987 | TE: | AB | RLD: | No |
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