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Last Updated: May 21, 2024

Suppliers and packages for generic ingredient: OXYCODONE HYDROCHLORIDE


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OXYCODONE HYDROCHLORIDE

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Specgx Llc ROXICODONE oxycodone hydrochloride TABLET;ORAL 021011 NDA SpecGx LLC 23635-581-10 100 TABLET in 1 BOTTLE, PLASTIC (23635-581-10) 2000-08-31
Specgx Llc ROXICODONE oxycodone hydrochloride TABLET;ORAL 021011 NDA SpecGx LLC 23635-582-10 100 TABLET in 1 BOTTLE, PLASTIC (23635-582-10) 2000-08-31
Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride TABLET, EXTENDED RELEASE;ORAL 022272 NDA AUTHORIZED GENERIC Teva Pharmaceuticals USA, Inc. 0093-5731-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5731-01) 2015-10-12
Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride TABLET, EXTENDED RELEASE;ORAL 022272 NDA AUTHORIZED GENERIC Teva Pharmaceuticals USA, Inc. 0093-5732-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5732-01) 2015-10-12
Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride TABLET, EXTENDED RELEASE;ORAL 022272 NDA AUTHORIZED GENERIC Teva Pharmaceuticals USA, Inc. 0093-5733-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5733-01) 2015-10-14
Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride TABLET, EXTENDED RELEASE;ORAL 022272 NDA AUTHORIZED GENERIC Teva Pharmaceuticals USA, Inc. 0093-5734-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-5734-01) 2015-10-14
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

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