Product Details for ANDA 087695
FOLEX (METHOTREXATE SODIUM)
EQ 25MG BASE/VIAL
Marketing Status: Discontinued
EQ 50MG BASE/VIAL
Marketing Status: Discontinued
EQ 100MG BASE/VIAL
Marketing Status: Discontinued
EQ 25MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: METHOTREXATE SODIUM
Proprietary Name: FOLEX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 25MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: A087695
Product Number: 001
Approval Date: Apr 8, 1983
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information
FOLEX (METHOTREXATE SODIUM)
Proprietary Name: FOLEX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 25MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: A087695
Product Number: 001
Approval Date: Apr 8, 1983
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 50MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: METHOTREXATE SODIUM
Proprietary Name: FOLEX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 50MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A087695
Product Number: 002
Approval Date: Apr 8, 1983
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information
FOLEX (METHOTREXATE SODIUM)
Proprietary Name: FOLEX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 50MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A087695
Product Number: 002
Approval Date: Apr 8, 1983
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 100MG BASE/VIAL
Marketing Status: Discontinued
Active Ingredient: METHOTREXATE SODIUM
Proprietary Name: FOLEX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 100MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: A087695
Product Number: 003
Approval Date: Apr 8, 1983
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: FOLEX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 100MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: A087695
Product Number: 003
Approval Date: Apr 8, 1983
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status: Discontinued
Patent and Exclusivity Information