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Oxycodone Hydrochloride - 68462-204-01 - (Oxycodone Hydrochloride)

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Drug Information of Oxycodone Hydrochloride

Product NDC: 68462-204
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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone Hydrochloride

Product NDC: 68462-204
Labeler Name: Glenmark Generics, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA200534
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20101215

Package Information of Oxycodone Hydrochloride

Package NDC: 68462-204-01
Package Description: 100 CAPSULE in 1 BOTTLE (68462-204-01)

NDC Information of Oxycodone Hydrochloride

NDC Code 68462-204-01
Proprietary Name Oxycodone Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (68462-204-01)
Product NDC 68462-204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101215
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Glenmark Generics, 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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