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Data / Drug companies / Opmx LLC

Opmx LLC: 97 products in the FDA NDC directory, labeler code 69729

Opmx LLC (labeler code 69729) lists 97 products in the FDA National Drug Code Directory, covering 22 finished drugs by generic name. By type: 97 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on September 7, 2026.

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Labeler code
69729
Products in commercial distribution
97
Packages
121
Finished drugs by generic name
22
Prescription products
0
Over the counter products
97
Flagged as original packager
21 of 21 products that carry the flag
Started marketing in the last 12 months
28
Earliest marketing start
February 10, 2016
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 drugs9294.8%
Generic drugs (ANDA)55.2%

Products by type

TypeProductsShare
Over the counter drugs97100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule, liquid filled2020.6%
Tablet1919.6%
Syrup1818.6%
Suspension1010.3%
Cream99.3%
Tablet, film coated88.2%
Tablet, coated66.2%
Tablet, chewable22.1%
Ointment22.1%
Capsule, delayed release11%
Capsule11%
Capsule, gelatin coated11%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tabcin Extra Strength69729-836Capsule, liquid filledOver the counter monograph drugsSeptember 7, 2026
Desenfriol-ito plus69729-835SuspensionOver the counter monograph drugsSeptember 5, 2026
Pentrexcilina69729-824SuspensionOver the counter monograph drugsSeptember 3, 2026
Mejoralito69729-823SuspensionOver the counter monograph drugsSeptember 3, 2026
Barmicil Plus69729-834CreamOver the counter monograph drugsJuly 27, 2026
Cardiaspirin protect69729-104Tablet, coatedOver the counter monograph drugsJuly 21, 2026
Viro Flu PM Relief69729-833Capsule, liquid filledOver the counter monograph drugsJuly 14, 2026
Barmicil Plus69729-830CreamOver the counter monograph drugsJuly 9, 2026
Quadriderm NF69729-828CreamOver the counter monograph drugsJuly 9, 2026
Diprospan69729-794CreamOver the counter monograph drugsJuly 9, 2026
Agrifen69729-816Capsule, liquid filledOver the counter monograph drugsJuly 8, 2026
Viro-Flu AM69729-831Capsule, liquid filledOver the counter monograph drugsJune 25, 2026
Desenfriol d69729-829TabletOver the counter monograph drugsJune 18, 2026
Neo-Lubrina Children69729-827SyrupOver the counter monograph drugsJune 17, 2026
Mejoralito Children69729-825SyrupOver the counter monograph drugsJune 16, 2026
Desenfriol-ito plus69729-815SyrupOver the counter monograph drugsJune 15, 2026
Buscapina69729-818Tablet, coatedOver the counter monograph drugsMarch 11, 2026
Riopan69729-791Capsule, delayed releaseGeneric drugs (ANDA)March 4, 2026
Tabcin ACTIVE69729-809Capsule, liquid filledOver the counter monograph drugsJanuary 30, 2026
Dolodol69729-601TabletOver the counter monograph drugsJanuary 30, 2026
Resfriol-ito Children69729-161Tablet, chewableOver the counter monograph drugsJanuary 30, 2026
Mejoralito Children CHILDREN69729-160Tablet, chewableOver the counter monograph drugsJanuary 30, 2026
Viro-Flu AM Relief69729-056Capsule, liquid filledOver the counter monograph drugsJanuary 30, 2026
Coldtac Severe Cold Max Relief69729-808Capsule, liquid filledOver the counter monograph drugsJanuary 29, 2026
Crocin MAX69729-801Capsule, gelatin coatedOver the counter monograph drugsJanuary 29, 2026

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.