16590-039 NDC - CARISOPRODOL ()

Drug Information

  • Product NDC: 16590-039
  • Proprietary Name: CARISOPRODOL
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: STAT RX USA LLC
Product Type:
FDA Application Number: ANDA040124
Marketing Category: ANDA
Start Marketing Date:1/24/1996

Package Information

No. Package Code Package Description Billing Unit
116590-039-2020 TABLET in 1 BOTTLE (16590-039-20)EA
216590-039-2828 TABLET in 1 BOTTLE (16590-039-28)EA
316590-039-3030 TABLET in 1 BOTTLE (16590-039-30)EA
416590-039-4040 TABLET in 1 BOTTLE (16590-039-40)EA
516590-039-4545 TABLET in 1 BOTTLE (16590-039-45)EA
616590-039-5656 TABLET in 1 BOTTLE (16590-039-56)EA
716590-039-6060 TABLET in 1 BOTTLE (16590-039-60)EA
816590-039-6284 TABLET in 1 BOTTLE (16590-039-62)EA
916590-039-7272 TABLET in 1 BOTTLE (16590-039-72)EA
1016590-039-82180 TABLET in 1 BOTTLE (16590-039-82)
1116590-039-84240 TABLET in 1 BOTTLE (16590-039-84)
1216590-039-9090 TABLET in 1 BOTTLE (16590-039-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC16590-039The 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 NAMECARISOPRODOLThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/24/1996This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct 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.
APPLICATION NUMBERANDA040124This 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.
LABELER NAMESTAT RX USA LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/4/2025

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