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Data / Drug companies / Phoenix RX LLC

Phoenix RX LLC: 61 products in the FDA NDC directory, labeler code 85509

Phoenix RX LLC (labeler code 85509) lists 61 products in the FDA National Drug Code Directory, covering 28 finished drugs by generic name. By type: 61 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on July 30, 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
85509
Products in commercial distribution
61
Packages
171
Finished drugs by generic name
28
Prescription products
61
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
August 17, 1981
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)5793.4%
Authorized generics (NDA)34.9%
Other unapproved drugs11.6%

Products by type

TypeProductsShare
Prescription drugs61100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet1524.6%
Tablet, film coated1321.3%
Tablet, delayed release813.1%
Solution69.8%
Capsule58.2%
Ointment46.6%
Patch34.9%
Capsule, delayed release23.3%
Capsule, extended release23.3%
System11.6%
Tablet, coated11.6%
Gel11.6%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Omeprazole and Sodium Bicarbonate85509-1032CapsuleGeneric drugs (ANDA)July 30, 2025
Methocarbamol85509-2910TabletGeneric drugs (ANDA)May 22, 2025
Cyclobenzaprine hydrochloride85509-1014Tablet, film coatedGeneric drugs (ANDA)March 20, 2025
Omeprazole85509-1644Capsule, delayed releaseGeneric drugs (ANDA)March 6, 2025
Diclofenac Potassium85509-1900Tablet, film coatedGeneric drugs (ANDA)November 1, 2024
Diclofenac Potassium85509-2750Tablet, film coatedGeneric drugs (ANDA)October 21, 2024
Ibuprofen85509-2396Tablet, film coatedGeneric drugs (ANDA)May 23, 2024
Diclofenac Sodium85509-1537SolutionGeneric drugs (ANDA)February 19, 2024
Naproxen and esomeprazole magnesium85509-1438Tablet, delayed releaseGeneric drugs (ANDA)October 11, 2023
Trubrexa85509-4000PatchOther unapproved drugsOctober 3, 2023
Diclofenac Sodium85509-1369SolutionGeneric drugs (ANDA)May 31, 2023
Ibuprofen and famotidine85509-1315TabletGeneric drugs (ANDA)March 15, 2023
Diclofenac Epolamine85509-1405SystemAuthorized generics (NDA)November 18, 2022
Naproxen and esomeprazole magnesium85509-1203Tablet, delayed releaseGeneric drugs (ANDA)October 6, 2022
Naproxen and esomeprazole magnesium85509-1202Tablet, delayed releaseGeneric drugs (ANDA)October 6, 2022
Diclofenac Sodium85509-1581GelGeneric drugs (ANDA)September 15, 2022
Diclofenac Sodium85509-2406SolutionGeneric drugs (ANDA)May 9, 2022
Diclofenac Sodium85509-1406SolutionGeneric drugs (ANDA)May 9, 2022
Gabapentin85509-1166TabletGeneric drugs (ANDA)October 1, 2021
Ibuprofen and famotidine85509-1626Tablet, film coatedGeneric drugs (ANDA)August 4, 2021
Ibuprofen and famotidine85509-1010Tablet, film coatedGeneric drugs (ANDA)August 4, 2021
Diclofenac Sodium 1.5%85509-1038SolutionGeneric drugs (ANDA)June 4, 2021
Methocarbamol85509-1910TabletGeneric drugs (ANDA)January 1, 2021
Celecoxib85509-1158CapsuleGeneric drugs (ANDA)December 3, 2020
Celecoxib85509-1237CapsuleGeneric drugs (ANDA)September 3, 2020

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.