50090-1801 NDC - BACLOFEN ()

Drug Information

  • Product NDC: 50090-1801
  • Proprietary Name: Baclofen
  • 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: ANDA077068
Marketing Category: ANDA
Start Marketing Date:8/30/2005

Package Information

No. Package Code Package Description Billing Unit
150090-1801-160 TABLET in 1 BOTTLE (50090-1801-1)EA
250090-1801-230 TABLET in 1 BOTTLE (50090-1801-2)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-1801The 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 NAMEBaclofenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/30/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAThe 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.
APPLICATION NUMBERANDA077068Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
LABELER NAMEA-S Medication SolutionsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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This page was last updated on: 12/19/2025