Visitor Monitoring Drug Details: METHOTREXATE LPF
 
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Drug Details

Drug Name: METHOTREXATE LPF
FDA Application No: (NDA) 011719
Active Ingredient(s): METHOTREXATE SODIUM
Company: HOSPIRA
Original Approval or Tentative Approval Date: August 10, 1959
Chemical Type: 2 New active ingredient
Review Classification: S Standard review drug
O Orphan drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
METHOTREXATE LPF METHOTREXATE SODIUMEQ 25MG BASE/MLINJECTABLE; INJECTION Discontinued No None
METHOTREXATE PRESERVATIVE FREE METHOTREXATE SODIUMEQ 2.5GM BASE/100ML (25 MG/ML)INJECTABLE; INJECTION Discontinued No None
METHOTREXATE PRESERVATIVE FREE METHOTREXATE SODIUMEQ 500MG BASE/20ML (25 MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None
METHOTREXATE PRESERVATIVE FREE METHOTREXATE SODIUMEQ 20MG BASE/2ML (10 MG/ML)INJECTABLE; INJECTION Discontinued No None
METHOTREXATE SODIUM METHOTREXATE SODIUMEQ 50MG BASE/2ML (25 MG/ML)INJECTABLE; INJECTION Prescription Yes AP
METHOTREXATE SODIUM METHOTREXATE SODIUMEQ 20MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
METHOTREXATE SODIUM METHOTREXATE SODIUMEQ 50MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
METHOTREXATE SODIUM METHOTREXATE SODIUMEQ 2.5MG BASE/MLINJECTABLE; INJECTION Discontinued No None
METHOTREXATE SODIUM METHOTREXATE SODIUMEQ 25MG BASE/MLINJECTABLE; INJECTION Discontinued No None
METHOTREXATE SODIUM METHOTREXATE SODIUMEQ 100MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
METHOTREXATE SODIUM PRESERVATIVE FREE METHOTREXATE SODIUMEQ 1GM BASE/40ML (25MG/ML)INJECTABLE; INJECTION Prescription Yes AP
METHOTREXATE SODIUM PRESERVATIVE FREE METHOTREXATE SODIUMEQ 1GM BASE/VIALINJECTABLE; INJECTION Discontinued No None


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