Details for New Drug Application (NDA): 065046
✉ Email this page to a colleague
The generic ingredient in CEFUROXIME SODIUM is cefuroxime sodium. There is one drug master file entry for this compound. Three suppliers are listed for this compound. Additional details are available on the cefuroxime sodium profile page.
Summary for 065046
| Tradename: | CEFUROXIME SODIUM |
| Applicant: | Hikma |
| Ingredient: | cefuroxime sodium |
| Patents: | 0 |
Suppliers and Packaging for NDA: 065046
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CEFUROXIME SODIUM | cefuroxime sodium | INJECTABLE;INJECTION | 065046 | ANDA | Hikma Pharmaceuticals USA Inc. | 0143-9569 | 0143-9569-10 | 10 VIAL in 1 CARTON (0143-9569-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9569-01) |
| CEFUROXIME SODIUM | cefuroxime sodium | INJECTABLE;INJECTION | 065046 | ANDA | Hikma Pharmaceuticals USA Inc. | 0143-9976 | 0143-9976-03 | 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0143-9976-03) / 82.5 mL in 1 VIAL, PHARMACY BULK PACKAGE (0143-9976-91) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | EQ 7.5GM BASE/VIAL | ||||
| Approval Date: | Jan 9, 2004 | TE: | RLD: | No | |||||
Complete Access Available with Subscription
