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

Golden State Medical Supply, Inc.: 59 products in the FDA NDC directory, labeler code 84677

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

Golden State Medical Supply, Inc. (labeler code 84677) lists 59 products in the FDA National Drug Code Directory, covering 17 finished drugs by generic name. By type: 59 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on June 25, 2026.

The request: Watch Golden State Medical Supply, Inc. (FDA labeler code 84677): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
84677
Products in commercial distribution
59
Packages
84
Finished drugs by generic name
17
Prescription products
59
Over the counter products
0
Flagged as original packager
6 of 6 products that carry the flag
Started marketing in the last 12 months
23
Earliest marketing start
December 20, 2006
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)59100%

Products by type

TypeProductsShare
Prescription drugs59100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet, film coated2033.9%
Tablet1728.8%
Capsule, extended release915.3%
Capsule711.9%
Tablet, film coated, extended release46.8%
Capsule, delayed release23.4%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tofacitinib citrate84677-081Tablet, film coated, extended releaseGeneric drugs (ANDA)June 25, 2026
Pioglitazone hydrochloride84677-028TabletGeneric drugs (ANDA)June 20, 2026
Pioglitazone hydrochloride84677-027TabletGeneric drugs (ANDA)June 20, 2026
Pioglitazone hydrochloride84677-026TabletGeneric drugs (ANDA)June 20, 2026
Dextromethorphan Hydrobromide and Quinidine Sulphate84677-067CapsuleGeneric drugs (ANDA)June 3, 2026
Tofacitinib84677-055Tablet, film coatedGeneric drugs (ANDA)June 1, 2026
Tofacitinib84677-054Tablet, film coatedGeneric drugs (ANDA)June 1, 2026
Sitagliptin and Metformin Hydrochloride84677-053Tablet, film coatedGeneric drugs (ANDA)April 30, 2026
Sitagliptin and Metformin Hydrochloride84677-052Tablet, film coatedGeneric drugs (ANDA)April 30, 2026
Valsartan and hydrochlorothiazide84677-076Tablet, film coatedGeneric drugs (ANDA)April 23, 2026
Valsartan and hydrochlorothiazide84677-075Tablet, film coatedGeneric drugs (ANDA)April 23, 2026
Valsartan and hydrochlorothiazide84677-074Tablet, film coatedGeneric drugs (ANDA)April 23, 2026
Valsartan and hydrochlorothiazide84677-073Tablet, film coatedGeneric drugs (ANDA)April 23, 2026
Valsartan and hydrochlorothiazide84677-072Tablet, film coatedGeneric drugs (ANDA)April 23, 2026
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE84677-058Tablet, film coatedGeneric drugs (ANDA)March 31, 2026
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE84677-057Tablet, film coatedGeneric drugs (ANDA)March 31, 2026
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE84677-056Tablet, film coatedGeneric drugs (ANDA)March 31, 2026
Dapagliflozin and Metformin Hydrochloride84677-022Tablet, film coated, extended releaseGeneric drugs (ANDA)March 16, 2026
Dapagliflozin and Metformin Hydrochloride84677-021Tablet, film coated, extended releaseGeneric drugs (ANDA)March 16, 2026
Dapagliflozin and Metformin Hydrochloride84677-020Tablet, film coated, extended releaseGeneric drugs (ANDA)March 16, 2026
Sitagliptin84677-051Tablet, film coatedGeneric drugs (ANDA)January 20, 2026
Sitagliptin84677-050Tablet, film coatedGeneric drugs (ANDA)January 20, 2026
Sitagliptin84677-049Tablet, film coatedGeneric drugs (ANDA)January 20, 2026
Lamotrigine84677-034TabletGeneric drugs (ANDA)October 7, 2025
Lamotrigine84677-033TabletGeneric drugs (ANDA)October 7, 2025

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.