Product Details for NDA 050571
CEFMAX (CEFMENOXIME 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: CEFMENOXIME HYDROCHLORIDE
Proprietary Name: CEFMAX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050571
Product Number: 001
Approval Date: Dec 30, 1987
Applicant Holder Full Name: TAP PHARMACEUTICAL PRODUCTS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
CEFMAX (CEFMENOXIME HYDROCHLORIDE)
Proprietary Name: CEFMAX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050571
Product Number: 001
Approval Date: Dec 30, 1987
Applicant Holder Full Name: TAP PHARMACEUTICAL PRODUCTS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 1GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFMENOXIME HYDROCHLORIDE
Proprietary Name: CEFMAX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050571
Product Number: 002
Approval Date: Dec 30, 1987
Applicant Holder Full Name: TAP PHARMACEUTICAL PRODUCTS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
CEFMAX (CEFMENOXIME HYDROCHLORIDE)
Proprietary Name: CEFMAX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050571
Product Number: 002
Approval Date: Dec 30, 1987
Applicant Holder Full Name: TAP PHARMACEUTICAL PRODUCTS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 2GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CEFMENOXIME HYDROCHLORIDE
Proprietary Name: CEFMAX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050571
Product Number: 003
Approval Date: Dec 30, 1987
Applicant Holder Full Name: TAP PHARMACEUTICAL PRODUCTS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: CEFMAX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050571
Product Number: 003
Approval Date: Dec 30, 1987
Applicant Holder Full Name: TAP PHARMACEUTICAL PRODUCTS INC
Marketing Status: Discontinued
Patent and Exclusivity Information