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Data / Drug companies / Golden State Medical Supply, Inc.

Golden State Medical Supply, Inc.: 102 products in the FDA NDC directory, labeler code 60429

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

Golden State Medical Supply, Inc. (labeler code 60429) lists 102 products in the FDA National Drug Code Directory, covering 46 finished drugs by generic name. By type: 99 prescription drugs, 3 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on June 30, 2021.

The request: Watch Golden State Medical Supply, Inc. (FDA labeler code 60429): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
60429
Products in commercial distribution
102
Packages
145
Finished drugs by generic name
46
Prescription products
99
Over the counter products
3
Controlled substance products
Schedule II 1, Schedule IV 9
Flagged as original packager
3 of 3 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
8
Earliest marketing start
August 25, 1986
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)9391.2%
New drug applications (NDA)98.8%

Products by type

TypeProductsShare
Prescription drugs9997.1%
Over the counter drugs32.9%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet4039.2%
Tablet, film coated2827.5%
Capsule1211.8%
Tablet, extended release87.8%
Tablet, delayed release43.9%
Patch, extended release32.9%
Spray, metered22%
Tablet, film coated, extended release22%
Tablet, chewable11%
Solution11%
Capsule, extended release11%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Icosapent Ethyl60429-005CapsuleGeneric drugs (ANDA)June 30, 2021
Ezetimibe60429-982TabletGeneric drugs (ANDA)June 12, 2017
Nitroglycerin60429-841TabletGeneric drugs (ANDA)August 26, 2016
Nitroglycerin60429-840TabletGeneric drugs (ANDA)August 26, 2016
Nitroglycerin60429-839TabletGeneric drugs (ANDA)August 26, 2016
Mometasone furoate60429-664Spray, meteredGeneric drugs (ANDA)March 22, 2016
Guanfacine Extended-Release60429-962Tablet, extended releaseGeneric drugs (ANDA)June 2, 2015
Guanfacine Extended-Release60429-961Tablet, extended releaseGeneric drugs (ANDA)June 2, 2015
Guanfacine Extended-Release60429-960Tablet, extended releaseGeneric drugs (ANDA)June 2, 2015
Donepezil Hydrochloride60429-322Tablet, film coatedGeneric drugs (ANDA)October 29, 2014
Donepezil Hydrochloride60429-321Tablet, film coatedGeneric drugs (ANDA)October 29, 2014
Pramipexole Dihydrochloride60429-090TabletGeneric drugs (ANDA)October 28, 2014
Pramipexole Dihydrochloride60429-089TabletGeneric drugs (ANDA)October 28, 2014
Pramipexole Dihydrochloride60429-088TabletGeneric drugs (ANDA)October 28, 2014
Pramipexole Dihydrochloride60429-087TabletGeneric drugs (ANDA)October 28, 2014
Pramipexole Dihydrochloride60429-086TabletGeneric drugs (ANDA)October 28, 2014
Pramipexole Dihydrochloride60429-085TabletGeneric drugs (ANDA)October 28, 2014
Mycophenolic Acid60429-017Tablet, delayed releaseGeneric drugs (ANDA)August 19, 2014
Nifedipine60429-049Tablet, extended releaseGeneric drugs (ANDA)April 3, 2014
Nifedipine60429-048Tablet, extended releaseGeneric drugs (ANDA)April 3, 2014
Nifedipine60429-047Tablet, extended releaseGeneric drugs (ANDA)April 3, 2014
Glycopyrrolate60429-666TabletGeneric drugs (ANDA)February 3, 2014
Metformin hydrochloride60429-113TabletGeneric drugs (ANDA)September 11, 2013
Metformin hydrochloride60429-112TabletGeneric drugs (ANDA)September 11, 2013
Metformin hydrochloride60429-111TabletGeneric drugs (ANDA)September 11, 2013

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.