60429-504 NDC - ALPRAZOLAM ()

Drug Information

  • Product NDC: 60429-504
  • Proprietary Name: Alprazolam
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Golden State Medical Supply Inc
Product Type:
FDA Application Number: ANDA074174
Marketing Category: ANDA
Start Marketing Date:3/28/2007
End Marketing Date:6/30/2022

Package Information

No. Package Code Package Description Billing Unit
160429-504-01100 TABLET in 1 BOTTLE (60429-504-01)
260429-504-05500 TABLET in 1 BOTTLE (60429-504-05)
360429-504-101000 TABLET in 1 BOTTLE (60429-504-10)
460429-504-12120 TABLET in 1 BOTTLE (60429-504-12)EA
560429-504-15150 TABLET in 1 BOTTLE (60429-504-15)EA
660429-504-18180 TABLET in 1 BOTTLE (60429-504-18)EA
760429-504-3030 TABLET in 1 BOTTLE (60429-504-30)EA
860429-504-6060 TABLET in 1 BOTTLE (60429-504-60)EA
960429-504-9090 TABLET in 1 BOTTLE (60429-504-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC60429-504This is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAMEAlprazolamProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
START MARKETING DATE3/28/2007This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
END MARKETING DATE6/30/2022Name of Company corresponding to the labeler code segment of the Product NDC.
MARKETING CATEGORY NAMEANDAAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
APPLICATION NUMBERANDA074174 
LABELER NAMEGolden State Medical Supply Inc 

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

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