Details for New Drug Application (NDA): 207147
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The generic ingredient in OXACILLIN SODIUM is oxacillin sodium. There are thirty-eight drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the oxacillin sodium profile page.
Summary for 207147
Tradename: | OXACILLIN SODIUM |
Applicant: | Wockhardt Bio Ag |
Ingredient: | oxacillin sodium |
Patents: | 0 |
Suppliers and Packaging for NDA: 207147
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
OXACILLIN SODIUM | oxacillin sodium | INJECTABLE;INJECTION | 207147 | ANDA | Wockhardt USA LLC. | 64679-698 | 64679-698-01 | 10 VIAL in 1 CARTON (64679-698-01) / 20 mL in 1 VIAL (64679-698-02) |
OXACILLIN SODIUM | oxacillin sodium | INJECTABLE;INJECTION | 207147 | ANDA | Wockhardt USA LLC. | 64679-698 | 64679-698-03 | 1 VIAL in 1 CARTON (64679-698-03) / 20 mL in 1 VIAL (64679-698-02) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 1GM BASE/VIAL | ||||
Approval Date: | Jul 31, 2017 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 2GM BASE/VIAL | ||||
Approval Date: | Jul 31, 2017 | TE: | AP | RLD: | No |
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