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54868-3826 NDC - METHOTREXATE SODIUM ()

Drug Information

Product NDC: 54868-3826

Proprietary Name: Methotrexate Sodium

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Physicians Total Care, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/5/2007

Package Information

No. Package Code Package Description Billing Unit
154868-3826-016 TABLET in 1 BOTTLE, PLASTIC (54868-3826-0)EA
254868-3826-112 TABLET in 1 BOTTLE (54868-3826-1)EA
354868-3826-320 TABLET in 1 BOTTLE (54868-3826-3)EA
454868-3826-428 TABLET in 1 BOTTLE (54868-3826-4)EA
554868-3826-5100 TABLET in 1 BOTTLE (54868-3826-5)EA
654868-3826-650 TABLET in 1 BOTTLE (54868-3826-6)EA
754868-3826-730 TABLET in 1 BOTTLE (54868-3826-7)EA
854868-3826-840 TABLET in 1 BOTTLE (54868-3826-8)EA
954868-3826-92 TABLET in 1 BOTTLE (54868-3826-9)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC54868-3826The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMethotrexate SodiumThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/5/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPhysicians Total Care, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023
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