Skip to the page

Data / Drug companies / R J General Corporation

R J General Corporation: 21 products in the FDA NDC directory, labeler code 70264

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

R J General Corporation (labeler code 70264) lists 21 products in the FDA National Drug Code Directory, covering 14 finished drugs by generic name. By type: 21 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on November 12, 2024.

The request: Watch R J General Corporation (FDA labeler code 70264): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
70264
Products in commercial distribution
21
Packages
21
Finished drugs by generic name
14
Prescription products
0
Over the counter products
21
Started marketing in the last 12 months
0
Earliest marketing start
March 2, 2010
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 drugs1885.7%
New drug applications (NDA)314.3%

Products by type

TypeProductsShare
Over the counter drugs21100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet628.6%
Tablet, film coated628.6%
Tablet, coated314.3%
Capsule, liquid filled29.5%
Tablet, effervescent29.5%
Powder, for solution14.8%
Tablet, chewable14.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Theraflu Severe Cold Relief Daytime70264-047Powder, for solutionOver the counter monograph drugsNovember 12, 2024
Tums Antacid Chewy Bites70264-046TabletOver the counter monograph drugsNovember 11, 2024
Excedrin Extra Strength Headache70264-045Tablet, film coatedOver the counter monograph drugsNovember 11, 2024
Ibuprofen 200 mg70264-044Capsule, liquid filledOver the counter monograph drugsNovember 5, 2024
Ibuprofen 200 mg70264-043Capsule, liquid filledOver the counter monograph drugsNovember 4, 2024
Ibuprofen 200 mg70264-042Tablet, coatedOver the counter monograph drugsNovember 1, 2024
Ibuprofen 200 mg70264-041Tablet, coatedOver the counter monograph drugsNovember 1, 2024
Acetaminophen 250 mg and Ibuprofen 125 mg70264-040Tablet, film coatedOver the counter monograph drugsOctober 30, 2024
Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz70264-016Tablet, effervescentOver the counter monograph drugsMarch 16, 2023
Benadryl Allergy70264-024Tablet, film coatedOver the counter monograph drugsMarch 1, 2022
Pepcid Complete70264-034Tablet, chewableNew drug applications (NDA)January 9, 2022
Motrin ib70264-029Tablet, film coatedOver the counter monograph drugsMay 1, 2021
Tylenol pm extra strength70264-028Tablet, film coatedOver the counter monograph drugsMay 1, 2021
Tylenol extra strength70264-027TabletOver the counter monograph drugsMay 1, 2021
Tylenol sinus severe70264-026Tablet, coatedOver the counter monograph drugsMay 1, 2021
Tylenol cold and flu70264-025Tablet, film coatedOver the counter monograph drugsMay 1, 2021
Claritin70264-030TabletNew drug applications (NDA)March 1, 2021
Bayer Genuine Aspirin70264-013TabletOver the counter monograph drugsJuly 31, 2014
Aleve70264-011TabletNew drug applications (NDA)February 26, 2014
Midol complete70264-012TabletOver the counter monograph drugsFebruary 10, 2014
Alka-Seltzer Original70264-014Tablet, effervescentOver the counter monograph drugsMarch 2, 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.