Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 087695

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FOLEX (METHOTREXATE SODIUM)
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)
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)
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