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Oxycodone Hydrochloride - 68382-794-01 - (Oxycodone Hydrochloride)

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Drug Information of Oxycodone Hydrochloride

Product NDC: 68382-794
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: Oxycodone Hydrochloride
Active Ingredient(s): 10    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: 68382-794
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077290
Marketing Category: ANDA
Start Marketing Date: 20121226

Package Information of Oxycodone Hydrochloride

Package NDC: 68382-794-01
Package Description: 100 TABLET in 1 BOTTLE (68382-794-01)

NDC Information of Oxycodone Hydrochloride

NDC Code 68382-794-01
Proprietary Name Oxycodone Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (68382-794-01)
Product NDC 68382-794
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121226
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


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