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Data / Drug companies / PD-Rx Pharmaceuticals, Inc.

PD-Rx Pharmaceuticals, Inc.: 60 products in the FDA NDC directory, labeler code 55289

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

PD-Rx Pharmaceuticals, Inc. (labeler code 55289) lists 60 products in the FDA National Drug Code Directory, covering 50 finished drugs by generic name. By type: 52 prescription drugs, 8 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on March 27, 2021.

The request: Watch PD-Rx Pharmaceuticals, Inc. (FDA labeler code 55289): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
55289
Products in commercial distribution
60
Packages
260
Finished drugs by generic name
50
Prescription products
52
Over the counter products
8
Controlled substance products
Schedule IV 7
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
June 3, 1975
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)5490%
Over the counter monograph drugs610%

Products by type

TypeProductsShare
Prescription drugs5286.7%
Over the counter drugs813.3%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet2745%
Capsule1525%
Tablet, film coated1016.7%
Suppository23.3%
Tablet, film coated, extended release23.3%
Tablet, delayed release11.7%
Tablet, coated11.7%
Capsule, extended release11.7%
Tablet, chewable11.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Fiber Lax55289-949Tablet, film coatedOver the counter monograph drugsMarch 27, 2021
Loratadine Allergy Relief55289-728TabletGeneric drugs (ANDA)November 1, 2017
Docusate Sodium55289-493CapsuleOver the counter monograph drugsMarch 1, 2016
Diphenhydramine HCl55289-479CapsuleOver the counter monograph drugsFebruary 1, 2016
Phentermine Hydrochloride55289-701TabletGeneric drugs (ANDA)August 15, 2012
Phentermine Hydrochloride55289-791CapsuleGeneric drugs (ANDA)August 7, 2012
Phentermine Hydrochloride55289-624CapsuleGeneric drugs (ANDA)August 7, 2012
Erythromycin55289-075Tablet, film coatedGeneric drugs (ANDA)September 6, 2011
Chlorzoxazone55289-633TabletGeneric drugs (ANDA)August 22, 2011
Verapamil hydrochloride55289-723Tablet, film coated, extended releaseGeneric drugs (ANDA)September 17, 2009
Indomethacin55289-469Capsule, extended releaseGeneric drugs (ANDA)March 6, 2009
Paroxetine55289-053Tablet, film coatedGeneric drugs (ANDA)March 24, 2008
Paroxetine55289-037Tablet, film coatedGeneric drugs (ANDA)March 24, 2008
Cetirizine Hydrochloride55289-995TabletGeneric drugs (ANDA)December 27, 2007
Lovastatin55289-692TabletGeneric drugs (ANDA)November 1, 2007
Famciclovir55289-168Tablet, film coatedGeneric drugs (ANDA)September 5, 2007
Paroxetine55289-972Tablet, film coatedGeneric drugs (ANDA)April 13, 2007
Meloxicam55289-272TabletGeneric drugs (ANDA)March 7, 2007
Acetaminophen Regular strength55289-563TabletOver the counter monograph drugsJanuary 9, 2007
Gabapentin55289-959TabletGeneric drugs (ANDA)April 1, 2006
Fluconazole55289-824TabletGeneric drugs (ANDA)January 25, 2006
Lisinopril55289-884TabletGeneric drugs (ANDA)January 13, 2006
Acetaminophen55289-880TabletOver the counter monograph drugsJanuary 10, 2006
Nifedipine55289-798Tablet, film coated, extended releaseGeneric drugs (ANDA)November 21, 2005
Metoprolol Tartrate55289-382Tablet, film coatedGeneric drugs (ANDA)February 23, 2004

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.