Product Details for ANDA 090291
CEFEPIME HYDROCHLORIDE (CEFEPIME HYDROCHLORIDE)
EQ 500MG BASE/VIAL
Marketing Status: Discontinued
EQ 1GM BASE/VIAL
Marketing Status: Discontinued
EQ 2GM BASE/VIAL
Marketing Status: Discontinued
EQ 500MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFEPIME HYDROCHLORIDE
Proprietary Name: CEFEPIME HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090291
Product Number: 001
Approval Date: Dec 21, 2010
Applicant Holder Full Name: FOSUN PHARMA USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
CEFEPIME HYDROCHLORIDE (CEFEPIME HYDROCHLORIDE)
Proprietary Name: CEFEPIME HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090291
Product Number: 001
Approval Date: Dec 21, 2010
Applicant Holder Full Name: FOSUN PHARMA USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 1GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFEPIME HYDROCHLORIDE
Proprietary Name: CEFEPIME HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090291
Product Number: 002
Approval Date: Dec 21, 2010
Applicant Holder Full Name: FOSUN PHARMA USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
CEFEPIME HYDROCHLORIDE (CEFEPIME HYDROCHLORIDE)
Proprietary Name: CEFEPIME HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090291
Product Number: 002
Approval Date: Dec 21, 2010
Applicant Holder Full Name: FOSUN PHARMA USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 2GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFEPIME HYDROCHLORIDE
Proprietary Name: CEFEPIME HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090291
Product Number: 003
Approval Date: Dec 21, 2010
Applicant Holder Full Name: FOSUN PHARMA USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: CEFEPIME HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A090291
Product Number: 003
Approval Date: Dec 21, 2010
Applicant Holder Full Name: FOSUN PHARMA USA INC
Marketing Status: Discontinued
Patent and Exclusivity Information