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Data / Drug companies / Doc Rx

Doc Rx: 15 products in the FDA NDC directory, labeler code 69306

Doc Rx (labeler code 69306) lists 15 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 15 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 31, 2025.

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
69306
Products in commercial distribution
15
Packages
32
Finished drugs by generic name
10
Prescription products
15
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
July 19, 1978
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)1493.3%
Authorized generics (NDA)16.7%

Products by type

TypeProductsShare
Prescription drugs15100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet853.3%
Tablet, film coated533.3%
Tablet, delayed release16.7%
Capsule, extended release16.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Cyclobenzaprine Hydrochloride69306-872Tablet, film coatedGeneric drugs (ANDA)July 31, 2025
Methocarbamol69306-510TabletGeneric drugs (ANDA)May 22, 2025
Diclofenac Potassium69306-750Tablet, film coatedGeneric drugs (ANDA)October 21, 2024
Ibuprofen and famotidine69306-266Tablet, film coatedGeneric drugs (ANDA)August 4, 2021
Methocarbamol69306-500TabletGeneric drugs (ANDA)January 1, 2021
Naproxen and esomeprazole magnesium69306-005Tablet, delayed releaseGeneric drugs (ANDA)February 18, 2020
Metaxalone69306-100TabletGeneric drugs (ANDA)April 1, 2019
Azithromycin69306-250Tablet, film coatedGeneric drugs (ANDA)March 12, 2019
Cyclobenzaprine Hydrochloride69306-015Capsule, extended releaseAuthorized generics (NDA)March 4, 2019
Etodolac69306-020Tablet, film coatedGeneric drugs (ANDA)June 11, 2018
Methylprednisolone69306-400TabletGeneric drugs (ANDA)May 14, 2018
Metaxalone69306-311TabletGeneric drugs (ANDA)November 22, 2016
Dexamethasone69306-111TabletGeneric drugs (ANDA)September 15, 1983
Dexamethasone69306-112TabletGeneric drugs (ANDA)August 26, 1982
Dexamethasone69306-114TabletGeneric drugs (ANDA)July 19, 1978

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