NDC 63629-1472

Methotrexate Sodium

Methotrexate Sodium

Methotrexate Sodium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Methotrexate Sodium.

Product ID63629-1472_135c8bb3-c85a-483a-a1bf-e850f1e88806
NDC63629-1472
Product TypeHuman Prescription Drug
Proprietary NameMethotrexate Sodium
Generic NameMethotrexate Sodium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1994-08-01
Marketing CategoryANDA / ANDA
Application NumberANDA040054
Labeler NameBryant Ranch Prepack
Substance NameMETHOTREXATE SODIUM
Active Ingredient Strength3 mg/1
Pharm ClassesFolate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 63629-1472-1

30 TABLET in 1 BOTTLE, PLASTIC (63629-1472-1)
Marketing Start Date1994-08-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-1472-2 [63629147202]

Methotrexate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA040054
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1994-08-01
Marketing End Date2016-12-30

NDC 63629-1472-1 [63629147201]

Methotrexate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA040054
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1994-08-01
Marketing End Date2016-12-30

NDC 63629-1472-3 [63629147203]

Methotrexate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA040054
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1994-08-01
Marketing End Date2016-12-30

NDC 63629-1472-4 [63629147204]

Methotrexate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA040054
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1994-08-01
Marketing End Date2016-12-30

NDC 63629-1472-5 [63629147205]

Methotrexate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA040054
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-01-16
Marketing End Date2016-12-30

NDC 63629-1472-6 [63629147206]

Methotrexate Sodium TABLET
Marketing CategoryANDA
Application NumberANDA040054
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-01-16
Marketing End Date2016-12-30

Drug Details

NDC Crossover Matching brand name "Methotrexate Sodium" or generic name "Methotrexate Sodium"

NDCBrand NameGeneric Name
0054-4550Methotrexate SodiumMethotrexate Sodium
0054-8550Methotrexate SodiumMethotrexate Sodium
63629-1472Methotrexate SodiumMethotrexate Sodium
66758-040Methotrexate SodiumMethotrexate Sodium
66758-041Methotrexate SodiumMethotrexate Sodium
70518-2711Methotrexate SodiumMethotrexate Sodium
75840-111METHOTREXATE SODIUMMETHOTREXATE SODIUM
21695-111MethotrexateMethotrexate sodium
47335-235MethotrexateMethotrexate Sodium
50090-3418MethotrexateMethotrexate Sodium
63323-122MethotrexateMETHOTREXATE SODIUM
63323-123MethotrexateMETHOTREXATE SODIUM
70518-1251MethotrexateMethotrexate Sodium

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