Product Details for NDA 050306
GEOPEN (CARBENICILLIN DISODIUM)
EQ 1GM BASE/VIAL
Marketing Status: Discontinued
EQ 2GM BASE/VIAL
Marketing Status: Discontinued
EQ 5GM BASE/VIAL
Marketing Status: Discontinued
EQ 10GM BASE/VIAL
Marketing Status: Discontinued
EQ 30GM BASE/VIAL
Marketing Status: Discontinued
EQ 1GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CARBENICILLIN DISODIUM
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
GEOPEN (CARBENICILLIN DISODIUM)
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 2GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CARBENICILLIN DISODIUM
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
GEOPEN (CARBENICILLIN DISODIUM)
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 5GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CARBENICILLIN DISODIUM
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 5GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
GEOPEN (CARBENICILLIN DISODIUM)
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 5GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 10GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CARBENICILLIN DISODIUM
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 10GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 006
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
GEOPEN (CARBENICILLIN DISODIUM)
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 10GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 006
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 30GM BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: CARBENICILLIN DISODIUM
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 30GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: GEOPEN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 30GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N050306
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ROERIG DIV PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information