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Data / Drug companies / Basf Corporation

Basf Corporation: 17 products in the FDA NDC directory, labeler code 10117

Basf Corporation (labeler code 10117) lists 17 products in the FDA National Drug Code Directory. By type: 15 bulk ingredients, 2 drugs for further processing. Its main marketing category is bulk ingredients. The newest product started marketing on May 1, 2022.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
10117
Products in commercial distribution
17
Packages
21
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
January 1, 1980
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients1376.5%
Bulk ingredients for compounding211.8%
Drugs for further processing211.8%

Products by type

TypeProductsShare
Bulk ingredients1588.2%
Drugs for further processing211.8%

Dosage forms

Dosage formProductsShare
Powder1482.4%
Liquid317.6%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Zinc oxide10117-3011PowderBulk ingredientsMay 1, 2022
Zinc oxide10117-3010PowderBulk ingredientsMay 6, 2019
Zinc oxide10117-3009PowderDrugs for further processingMarch 31, 2019
Zinc oxide10117-3008PowderBulk ingredientsMay 12, 2014
Ibuprofen dc85w10117-0931PowderBulk ingredientsJanuary 2, 2014
Zinc oxide10117-3006PowderBulk ingredientsAugust 12, 2013
Zinc oxide10117-3007PowderBulk ingredientsMay 11, 2012
Ibuprofen10117-0952PowderBulk ingredientsJune 8, 2010
Ibuprofen10117-0936PowderBulk ingredients for compoundingJune 8, 2010
Ibuprofen10117-0930PowderBulk ingredients for compoundingJune 8, 2010
Ibuprofen10117-0926PowderBulk ingredientsJune 8, 2010
Sodium ibuprofen dihydrate10117-0990PowderBulk ingredientsApril 1, 2005
Octinoxate, avobenzone10117-3613LiquidDrugs for further processingJanuary 14, 2005
Zinc oxide10117-3004PowderBulk ingredientsMay 25, 2000
Zinc oxide10117-3003PowderBulk ingredientsMay 25, 2000
Poloxalene10117-2019LiquidBulk ingredientsJanuary 1, 1980
Poloxalene10117-0218LiquidBulk ingredientsJanuary 1, 1980

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.