Details for New Drug Application (NDA): 076870
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The generic ingredient in ALLOPURINOL SODIUM 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 076870
Tradename: | ALLOPURINOL SODIUM |
Applicant: | Hikma |
Ingredient: | allopurinol sodium |
Patents: | 0 |
Pharmacology for NDA: 076870
Mechanism of Action | Xanthine Oxidase Inhibitors |
Suppliers and Packaging for NDA: 076870
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ALLOPURINOL SODIUM | allopurinol sodium | INJECTABLE;INJECTION | 076870 | ANDA | Hikma Pharmaceuticals USA Inc. | 0143-9533 | 0143-9533-01 | 1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01) / 25 mL in 1 VIAL |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 500MG BASE/VIAL | ||||
Approval Date: | Aug 26, 2004 | TE: | AP | RLD: | No |
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