Details for New Drug Application (NDA): 064032
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The generic ingredient in TAZICEF is ceftazidime. There are seventeen drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the ceftazidime profile page.
Summary for 064032
Tradename: | TAZICEF |
Applicant: | Hospira |
Ingredient: | ceftazidime |
Patents: | 0 |
Suppliers and Packaging for NDA: 064032
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
TAZICEF | ceftazidime | INJECTABLE;INJECTION | 064032 | ANDA | Hospira, Inc. | 0409-5092 | 0409-5092-16 | 25 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-5092-16) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0409-5092-11) |
TAZICEF | ceftazidime | INJECTABLE;INJECTION | 064032 | ANDA | Hospira, Inc. | 0409-5093 | 0409-5093-11 | 10 VIAL, PATENT DELIVERY SYSTEM in 1 TRAY (0409-5093-11) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM (0409-5093-14) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 1GM/VIAL | ||||
Approval Date: | Oct 31, 1993 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2GM/VIAL | ||||
Approval Date: | Oct 31, 1993 | TE: | AP | RLD: | No |
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