82525-0010 NDC - TITANIUM DIOXIDE

Drug Information

  • Product NDC: 82525-0010
  • Proprietary Name:
  • Non Proprietary Name: titanium dioxide
  • Active Ingredient(s): .93 kg/kg TITANIUM DIOXIDE
  • Administration Route(s):
  • Dosage Form(s): POWDER

Labeler Information

Field Name Field Value
Labeler Name: TAEKYUNG SBC Co., LTD
Product Type: DRUG FOR FURTHER PROCESSING
FDA Application Number:
Marketing Category: DRUG FOR FURTHER PROCESSING
Start Marketing Date:2/18/2022

Package Information

No. Package Code Package Description Billing Unit
182525-0010-110 kg in 1 CARTON (82525-0010-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC82525-0010The 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.
PRODUCT TYPE NAMEDRUG FOR FURTHER PROCESSINGThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NON PROPRIETARY NAMEtitanium dioxideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPOWDERThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE2/18/2022The translation of the route code submitted by the firm, indicating route of administration.
MARKETING CATEGORY NAMEDRUG FOR FURTHER PROCESSINGThis is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETAEKYUNG SBC Co., LTDProduct 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.
SUBSTANCE NAMETITANIUM DIOXIDEThis 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.
ACTIVE NUMERATOR STRENGTH.93Name of Company corresponding to the labeler code segment of the Product NDC.
ACTIVE INGRED UNITkg/kg 

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This page was last updated on: 1/2/2026

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