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Data / Drug companies / Poly Pharmaceuticals, Inc.

Poly Pharmaceuticals, Inc.: 18 products in the FDA NDC directory, labeler code 50991

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

Poly Pharmaceuticals, Inc. (labeler code 50991) lists 18 products in the FDA National Drug Code Directory, covering 15 finished drugs by generic name. By type: 16 over the counter drugs, 2 prescription drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on April 23, 2026.

The request: Watch Poly Pharmaceuticals, Inc. (FDA labeler code 50991): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
50991
Products in commercial distribution
18
Packages
36
Finished drugs by generic name
15
Prescription products
2
Over the counter products
16
Controlled substance products
Schedule V 1
Flagged as original packager
18 of 18 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
August 22, 2011
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 drugs1688.9%
Generic drugs (ANDA)211.1%

Products by type

TypeProductsShare
Over the counter drugs1688.9%
Prescription drugs211.1%

Drugs it lists

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

DrugProductsCompanies listing it
Dextromethorphan hbr, phenylephrine hcl, pyrilamine maleate11
Dexchlorpheniramine maleate and dextromethorphan hbr11
Dextromethorphan hbr, pheniramine maleate, phenylephrine hcl11
Dexbrompheniramine maleate11
Dexbrompheniramine maleate, pseudoephedrine hcl12
Guaifenesin and pseudoephedrine hcl114
Dextromethorphan hbr, guaifenesin and pseudoephedrine hcl11
Pheniramine maleate, phenylephrine hcl11
Triprolidine hcl, dextromethorphan hbr11
Codeine phosphate, dexbrompheniramine maleate11
Tolmetin sodium15
Doxylamine succinate and phenylephrine hydrochloride11
Dexbrompheniramine maleate, phenylephrine hydrochloride11
Orphenadrine citrate, aspirin and caffeine13
Guaifenesin and phenylephrine hcl12

Dosage forms

Dosage formProductsShare
Tablet1055.6%
Liquid527.8%
Syrup15.6%
Tablet, film coated15.6%
Tablet, multilayer15.6%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Poly-hist dm50991-271LiquidOver the counter monograph drugsApril 23, 2026
Duratuss dm50991-142LiquidOver the counter monograph drugsOctober 15, 2025
Duratuss AC50991-540LiquidOver the counter monograph drugsSeptember 8, 2025
Durahist50991-865TabletOver the counter monograph drugsApril 22, 2025
Tolectin50991-988Tablet, film coatedGeneric drugs (ANDA)April 4, 2024
Alahist dm50991-444LiquidOver the counter monograph drugsJune 8, 2023
Polytussin DM50991-132SyrupOver the counter monograph drugsJune 8, 2023
Endal50991-136LiquidOver the counter monograph drugsMay 22, 2023
Alahist PE50991-788TabletOver the counter monograph drugsAugust 24, 2020
Alahist D50991-776TabletOver the counter monograph drugsApril 1, 2020
Deconex dmx50991-740TabletOver the counter monograph drugsJune 1, 2019
Poly Hist Forte50991-626TabletOver the counter monograph drugsJune 1, 2019
Norgesic Forte50991-999Tablet, multilayerGeneric drugs (ANDA)April 1, 2019
Deconex IR50991-736TabletOver the counter monograph drugsAugust 8, 2016
Duraflu50991-535TabletOver the counter monograph drugsOctober 1, 2015
Poly-Vent DM50991-214TabletOver the counter monograph drugsJune 17, 2013
Poly-Vent IR50991-212TabletOver the counter monograph drugsJune 11, 2013
Ala-hist ir50991-783TabletOver the counter monograph drugsAugust 22, 2011

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.