50090-4071 NDC - HYDROCODONE BITARTRATE AND ACETAMINOPHEN ()

Drug Information

  • Product NDC: 50090-4071
  • Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: A-S Medication Solutions
Product Type:
FDA Application Number: ANDA202991
Marketing Category: ANDA
Start Marketing Date:4/12/2016

Package Information

No. Package Code Package Description Billing Unit
150090-4071-020 TABLET in 1 BOTTLE (50090-4071-0)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-4071The 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 NAMEHydrocodone Bitartrate 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 DATE4/12/2016The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMEANDAThe translation of the dosage form Code submitted by the firm.
APPLICATION NUMBERANDA202991The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAMEA-S Medication SolutionsThis is the date that the labeler indicates was the start of its marketing of the drug product.

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This page was last updated on: 11/21/2025