50090-0919 NDC - TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN ()

Drug Information

Product NDC: 50090-0919

Proprietary Name: Tramadol Hydrochloride and Acetaminophen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: A-S Medication Solutions
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/17/2009

Package Information

No. Package Code Package Description Billing Unit
150090-0919-020 TABLET in 1 BOTTLE (50090-0919-0)
250090-0919-130 TABLET in 1 BOTTLE (50090-0919-1)
350090-0919-260 TABLET in 1 BOTTLE (50090-0919-2)
450090-0919-3120 TABLET in 1 BOTTLE (50090-0919-3)
550090-0919-490 TABLET in 1 BOTTLE (50090-0919-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-0919The 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 NAMETramadol Hydrochloride and AcetaminophenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/17/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEA-S Medication SolutionsName 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