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Data / Drug companies / Edwards Pharmaceuticals, Inc.

Edwards Pharmaceuticals, Inc.: 13 products in the FDA NDC directory, labeler code 0485

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

Edwards Pharmaceuticals, Inc. (labeler code 0485) lists 13 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 11 over the counter drugs, 2 prescription drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on October 27, 2014.

The request: Watch Edwards Pharmaceuticals, Inc. (FDA labeler code 0485): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
0485
Products in commercial distribution
13
Packages
14
Finished drugs by generic name
8
Prescription products
2
Over the counter products
11
Flagged as original packager
13 of 13 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
November 19, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Other unapproved drugs861.5%
Over the counter monograph drugs538.5%

Products by type

TypeProductsShare
Over the counter drugs1184.6%
Prescription drugs215.4%

Drugs it lists

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

DrugProductsCompanies listing it
Dexchlorpheniramine maleate and phenylephrine hydrochloride11
Chlorpheniramine maleate131
Brompheniramine maleate and pseudoephedrine hydrochloride11
Chlorpheniramine maleate and phenylephrine hydrochloride11
Guaifenesin and phenylephrine11
Brompheniramine maleate and phenylephrine hcl11
Acetaminophen1214
Chlorpheniramine/phenylephrine11

Dosage forms

Dosage formProductsShare
Liquid861.5%
Tablet, coated538.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ed-a-hist dm0485-0240Tablet, coatedOther unapproved drugsOctober 27, 2014
Ed a-hist dm0485-0171LiquidOver the counter monograph drugsSeptember 11, 2012
Ed bron gp0485-0208LiquidOther unapproved drugsJune 1, 2012
Ed apap0485-0057LiquidOver the counter monograph drugsMarch 7, 2012
Rymed0485-0080Tablet, coatedOver the counter monograph drugsNovember 15, 2011
Ed a-hist0485-0254Tablet, coatedOther unapproved drugsOctober 8, 2011
Rynex DM0485-0204LiquidOver the counter monograph drugsMarch 14, 2011
Rynex pse0485-0206LiquidOther unapproved drugsMarch 7, 2011
Rynex pe0485-0202LiquidOver the counter monograph drugsMarch 7, 2011
Ed chlorped jr0485-0098LiquidOther unapproved drugsMarch 4, 2011
Ed a-hist0485-0155LiquidOther unapproved drugsJanuary 11, 2011
Urogesic blue0485-0151Tablet, coatedOther unapproved drugsNovember 19, 2010
Urogesic blue0485-0151Tablet, coatedOther unapproved drugsNovember 19, 2010

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.