71205-133 NDC - SUDOGEST ()

Drug Information

  • Product NDC: 71205-133
  • Proprietary Name: SudoGest
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Proficient Rx LP
Product Type:
FDA Application Number: M012
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:8/25/1981
End Marketing Date:11/11/2021

Package Information

No. Package Code Package Description Billing Unit
171205-133-241 BLISTER PACK in 1 CARTON (71205-133-24) / 24 TABLET, FILM COATED in 1 BLISTER PACKEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC71205-133The 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 NAMESudoGestThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/25/1981The 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.
END MARKETING DATE11/11/2021Indicates 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.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM012This 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 NAMEProficient Rx LPName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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