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Data / Drug companies / Sci Pharmtech, Inc.

Sci Pharmtech, Inc.: 11 products in the FDA NDC directory, labeler code 68108

Sci Pharmtech, Inc. (labeler code 68108) lists 11 products in the FDA National Drug Code Directory. By type: 11 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on September 29, 2020.

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
68108
Products in commercial distribution
11
Packages
22
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule V 1
Started marketing in the last 12 months
0
Earliest marketing start
June 11, 2003
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients1090.9%
Bulk ingredients for compounding19.1%

Products by type

TypeProductsShare
Bulk ingredients11100%

Dosage forms

Dosage formProductsShare
Powder1090.9%
Liquid19.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Cannabidiol68108-0881PowderBulk ingredientsSeptember 29, 2020
Atomoxetine hydrochloride68108-0772PowderBulk ingredients for compoundingAugust 9, 2018
Brinzolamide68108-0821PowderBulk ingredientsJanuary 25, 2016
Hydroxychloroquine sulfate68108-0336PowderBulk ingredientsDecember 2, 2012
Articaine hydrochloride68108-0610PowderBulk ingredientsJune 21, 2012
Duloxetine hydrochloride68108-0705PowderBulk ingredientsJanuary 1, 2012
Propafenone hydrochloride68108-0340PowderBulk ingredientsJanuary 1, 2012
Divalproex sodium68108-0234PowderBulk ingredientsJanuary 1, 2012
Valproate sodium68108-0233PowderBulk ingredientsJune 23, 2004
Probucol68108-0304PowderBulk ingredientsJune 14, 2004
Valproic acid68108-0203LiquidBulk ingredientsJune 11, 2003

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.