Methotrexate Sodium

Product NDC
63629-1472
11-digit product format
636291472
Labeler code
63629
Product ID
63629-1472_271ff7a2-4904-a0ae-778e-0b5ec8e78d76
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Methotrexate Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040054
Marketing category
ANDA
Marketing start
1994-08-01
Marketing end
0000-00-00
Substance
METHOTREXATE SODIUM
Active strength
3 mg/1
Pharmacologic classes
Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-1472-1EA - Each63629-147284ecf7f4-cad5-4013-8aa4-f0fb819197b212012-07-24
63629-1472-2EA - Each63629-1472d19c5cae-6930-4760-8f12-bdf679bfd13e12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-1472-16362914720130 TABLET in 1 BOTTLE, PLASTIC (63629-1472-1) 30 tablet1994-08-010000-00-00NoNoCurrent
63629-1472-26362914720212 TABLET in 1 BOTTLE, PLASTIC (63629-1472-2) 12 tablet1994-08-010000-00-00NoNoCurrent
63629-1472-36362914720320 TABLET in 1 BOTTLE, PLASTIC (63629-1472-3) 20 tablet1994-08-010000-00-00NoNoCurrent
63629-1472-463629147204100 TABLET in 1 BOTTLE, PLASTIC (63629-1472-4) 100 tablet1994-08-010000-00-00NoNoCurrent
63629-1472-56362914720536 TABLET in 1 BOTTLE (63629-1472-5) 36 tablet2008-01-160000-00-00NoNoCurrent
63629-1472-66362914720624 TABLET in 1 BOTTLE (63629-1472-6) 24 tablet2008-01-160000-00-00NoNoCurrent
63629-1472-76362914720790 TABLET in 1 BOTTLE, PLASTIC (63629-1472-7) 90 tablet2021-09-200000-00-00NoNoCurrent
63629-1472-8636291472084 TABLET in 1 BOTTLE, PLASTIC (63629-1472-8) 4 tablet2021-09-200000-00-00NoNoCurrent