Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 065238

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CEFOXITIN (CEFOXITIN SODIUM)
EQ 1GM BASE/VIAL Marketing Status: Prescription

Active Ingredient: CEFOXITIN SODIUM
Proprietary Name: CEFOXITIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A065238
Product Number: 001
Approval Date: Mar 12, 2010
Applicant Holder Full Name: HIKMA FARMACEUTICA (PORTUGAL) SA
Marketing Status:  Prescription
Patent and Exclusivity Information

CEFOXITIN (CEFOXITIN SODIUM)
EQ 2GM BASE/VIAL Marketing Status: Prescription

Active Ingredient: CEFOXITIN SODIUM
Proprietary Name: CEFOXITIN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A065238
Product Number: 002
Approval Date: Mar 12, 2010
Applicant Holder Full Name: HIKMA FARMACEUTICA (PORTUGAL) SA
Marketing Status:  Prescription
Patent and Exclusivity Information

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