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Data / Drug companies / Pioneer Life Sciences, LLC

Pioneer Life Sciences, LLC: 77 products in the FDA NDC directory, labeler code 72090

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Pioneer Life Sciences, LLC (labeler code 72090) lists 77 products in the FDA National Drug Code Directory, covering 31 finished drugs by generic name. By type: 68 over the counter drugs, 9 drugs for further processing. Its main marketing category is over the counter monograph drugs. The newest product started marketing on August 12, 2026.

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Labeler code
72090
Products in commercial distribution
77
Packages
90
Finished drugs by generic name
31
Prescription products
0
Over the counter products
68
Flagged as original packager
61 of 61 products that carry the flag
Started marketing in the last 12 months
18
Products with a marketing end date set
1
Earliest marketing start
June 29, 2020
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs4963.6%
Generic drugs (ANDA)1722.1%
Drugs for further processing911.7%
Other unapproved drugs22.6%

Products by type

TypeProductsShare
Over the counter drugs6888.3%
Drugs for further processing911.7%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Tablet4963.6%
Capsule, liquid filled2228.6%
Tablet, extended release22.6%
Tablet, coated11.3%
Gel11.3%
Powder, for solution11.3%
Syrup11.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Gencare- Pain Relief Acetaminophen72090-069TabletOver the counter monograph drugsAugust 12, 2026
Gencare-Urinary Tract Defense72090-065TabletOther unapproved drugsAugust 10, 2026
Gencare-Gas Relief72090-073Capsule, liquid filledOver the counter monograph drugsAugust 4, 2026
Ibuprofen72090-071TabletGeneric drugs (ANDA)July 29, 2026
Ibuprofen72090-070TabletGeneric drugs (ANDA)July 29, 2026
Gencare-Urinary Pain Relief Maximum Strength72090-072TabletOther unapproved drugsJuly 21, 2026
Gencare-Allergy Relief72090-068TabletGeneric drugs (ANDA)June 22, 2026
Allergy Relief72090-028TabletGeneric drugs (ANDA)April 6, 2026
Gencare Long-Acting Cough Relief72090-063Capsule, liquid filledOver the counter monograph drugsMarch 24, 2026
Bisacodyl72090-131Tablet, coatedOver the counter monograph drugsMarch 2, 2026
Gas Relief72090-060Capsule, liquid filledOver the counter monograph drugsFebruary 25, 2026
Gencare DayTime Cold and Flu Softgel72090-062Capsule, liquid filledOver the counter monograph drugsFebruary 16, 2026
Gas Relief72090-015Capsule, liquid filledOver the counter monograph drugsFebruary 16, 2026
Gencare Hives Relief72090-058TabletGeneric drugs (ANDA)January 21, 2026
Mucus relief72090-044TabletOver the counter monograph drugsDecember 23, 2025
Mucus Relief72090-011Tablet, extended releaseGeneric drugs (ANDA)December 22, 2025
Mucus Relief72090-012Tablet, extended releaseGeneric drugs (ANDA)December 4, 2025
Gas Relief72090-014Capsule, liquid filledOver the counter monograph drugsNovember 19, 2025
Gencare-Senna-S Softgel72090-054Capsule, liquid filledOver the counter monograph drugsJune 30, 2025
Allergy Relief Diphenhydramine HCl 25mg SoftGel72090-052Capsule, liquid filledOver the counter monograph drugsJune 30, 2025
Gencare-Allergy Relief Loratadine Tablets, 10 mg72090-051TabletGeneric drugs (ANDA)June 30, 2025
Upset Stomach Relief-Bismuth Subsalicylate 262 mg72090-053Capsule, liquid filledOver the counter monograph drugsJune 27, 2025
Allergy relief72090-028TabletGeneric drugs (ANDA)June 1, 2025
Simethicone 125 mg72090-057Capsule, liquid filledDrugs for further processingMay 23, 2025
Acetaminophen 325mg, dextromethorphan hydrobromide 15mg and doxylamine succinate 6.25mg72090-056Capsule, liquid filledDrugs for further processingMay 23, 2025

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.