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Data / Drug companies / Richmond Pharmaceuticals, Inc.

Richmond Pharmaceuticals, Inc.: 27 products in the FDA NDC directory, labeler code 54738

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

Richmond Pharmaceuticals, Inc. (labeler code 54738) lists 27 products in the FDA National Drug Code Directory, covering 15 finished drugs by generic name. By type: 26 over the counter drugs, 1 prescription drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on November 21, 2024.

The request: Watch Richmond Pharmaceuticals, Inc. (FDA labeler code 54738): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
54738
Products in commercial distribution
27
Packages
46
Finished drugs by generic name
15
Prescription products
1
Over the counter products
26
Flagged as original packager
27 of 27 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
February 15, 2000
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 drugs2488.9%
Other unapproved drugs27.4%
Generic drugs (ANDA)13.7%

Products by type

TypeProductsShare
Over the counter drugs2696.3%
Prescription drugs13.7%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet1659.3%
Tablet, chewable622.2%
Capsule414.8%
Suspension13.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sucralfate54738-005SuspensionGeneric drugs (ANDA)November 21, 2024
Mucus Relief Cough and Congestion DM54738-985TabletOver the counter monograph drugsApril 1, 2016
Mucus Relief54738-981TabletOver the counter monograph drugsMarch 1, 2016
Mucus Relief54738-980TabletOver the counter monograph drugsMarch 1, 2016
Magnesium Oxide54738-974TabletOver the counter monograph drugsFebruary 1, 2016
Magnesium Oxide54738-973TabletOver the counter monograph drugsFebruary 1, 2016
Ferrous sulfate54738-963TabletOther unapproved drugsJune 1, 2015
Aspirin54738-541TabletOver the counter monograph drugsJune 1, 2015
Pepto Relief54738-102Tablet, chewableOver the counter monograph drugsJune 1, 2015
Sodium Bicarbonate Antacid54738-035TabletOver the counter monograph drugsJune 1, 2015
Acetaminophen54738-548TabletOver the counter monograph drugsMay 1, 2015
Diphenhydramine Hydrochloride54738-116CapsuleOver the counter monograph drugsMay 1, 2015
Diphenhydramine Hydrochloride54738-115CapsuleOver the counter monograph drugsMay 1, 2015
Aspirin54738-111TabletOver the counter monograph drugsMay 1, 2015
Anti Allergy54738-103TabletOver the counter monograph drugsMay 1, 2015
Antacid54738-030Tablet, chewableOver the counter monograph drugsMay 1, 2015
Meclizine HCL54738-025Tablet, chewableOver the counter monograph drugsMay 1, 2015
Sodium bicarbonate54738-020TabletOver the counter monograph drugsMay 1, 2015
Aspirin54738-559TabletOver the counter monograph drugsApril 1, 2015
Apap54738-540TabletOver the counter monograph drugsApril 1, 2015
Aspirin54738-128Tablet, chewableOver the counter monograph drugsApril 1, 2015
Chewable Acetaminophen Childrens54738-092Tablet, chewableOver the counter monograph drugsApril 1, 2015
Apap54738-040TabletOver the counter monograph drugsApril 1, 2015
Simethicone54738-518Tablet, chewableOver the counter monograph drugsMarch 1, 2011
Ferrous Sulfate54738-963TabletOther unapproved drugsNovember 5, 2008

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.