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Oxycodone Hydrochloride - 43063-304-30 - (Oxycodone Hydrochloride)

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Drug Information of Oxycodone Hydrochloride

Product NDC: 43063-304
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: Oxycodone Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Oxycodone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone Hydrochloride

Product NDC: 43063-304
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077712
Marketing Category: ANDA
Start Marketing Date: 20090302

Package Information of Oxycodone Hydrochloride

Package NDC: 43063-304-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-304-30)

NDC Information of Oxycodone Hydrochloride

NDC Code 43063-304-30
Proprietary Name Oxycodone Hydrochloride
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-304-30)
Product NDC 43063-304
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090302
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


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