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Last Updated: December 11, 2025

Pharmaceutical drugs supplied by: PHOENIX RX LLC


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PHOENIX RX LLC

Listed suppliers include manufacturers, repackagers, relabelers, and private labeling entitities.

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Sun Pharm Inds Ltd CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET;ORAL 078722 ANDA PHOENIX RX LLC 85509-1001-1 120 TABLET, FILM COATED in 1 BOTTLE (85509-1001-1) 2015-03-25
Sun Pharm Inds Ltd CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET;ORAL 078722 ANDA PHOENIX RX LLC 85509-1001-3 30 TABLET, FILM COATED in 1 BOTTLE (85509-1001-3) 2015-03-25
Sun Pharm Inds Ltd CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET;ORAL 078722 ANDA PHOENIX RX LLC 85509-1001-6 60 TABLET, FILM COATED in 1 BOTTLE (85509-1001-6) 2015-03-25
Sun Pharm Inds Ltd CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET;ORAL 078722 ANDA PHOENIX RX LLC 85509-1001-9 90 TABLET, FILM COATED in 1 BOTTLE (85509-1001-9) 2015-03-25
Alkem Labs Ltd IBUPROFEN AND FAMOTIDINE famotidine; ibuprofen TABLET;ORAL 211890 ANDA PHOENIX RX LLC 85509-1010-3 30 TABLET, FILM COATED in 1 BOTTLE (85509-1010-3) 2021-08-04
Alkem Labs Ltd IBUPROFEN AND FAMOTIDINE famotidine; ibuprofen TABLET;ORAL 211890 ANDA PHOENIX RX LLC 85509-1010-6 60 TABLET, FILM COATED in 1 BOTTLE (85509-1010-6) 2021-08-04
Alkem Labs Ltd IBUPROFEN AND FAMOTIDINE famotidine; ibuprofen TABLET;ORAL 211890 ANDA PHOENIX RX LLC 85509-1010-9 90 TABLET, FILM COATED in 1 BOTTLE (85509-1010-9) 2021-08-04
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

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Friedman, Yali. "DrugPatentWatch" DrugPatentWatch, thinkBiotech, 2025, www.DrugPatentWatch.com.
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