METHOTREXATE

Product NDC: 50090-0294
11-digit product format: 500900294
Labeler code: 50090
Product ID: 50090-0294_149eb9e1-d73b-4726-bea4-a577f4e002ed
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: METHOTREXATE
Dosage form: TABLET
Route: ORAL
Labeler: A-S Medication Solutions
Application: NDA008085
Marketing category: NDA
Marketing start: 1953-12-07
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: 2021-12-31
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50090-0294-9	EA - Each	50090-0294	8e212f6d-7c05-405a-9847-e7ced8553b7a	1	2018-08-13

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3IG1E710ZN	METHOTREXATE SODIUM	7413-34-5	METHOTREXATE SODIUM
YL5FZ2Y5U1	METHOTREXATE	59-05-2	METHOTREXATE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50090-0294-9	50090029409	36 TABLET in 1 BOTTLE (50090-0294-9)	36 tablet	2016-06-29	0000-00-00	No	No	Current