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Oxycodone Hydrochloride - 0527-1426-36 - (Oxycodone Hydrochloride)

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Drug Information of Oxycodone Hydrochloride

Product NDC: 0527-1426
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: Oxycodone Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Oxycodone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone Hydrochloride

Product NDC: 0527-1426
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20060101

Package Information of Oxycodone Hydrochloride

Package NDC: 0527-1426-36
Package Description: 1 BOTTLE in 1 CARTON (0527-1426-36) > 30 mL in 1 BOTTLE

NDC Information of Oxycodone Hydrochloride

NDC Code 0527-1426-36
Proprietary Name Oxycodone Hydrochloride
Package Description 1 BOTTLE in 1 CARTON (0527-1426-36) > 30 mL in 1 BOTTLE
Product NDC 0527-1426
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name SOLUTION, CONCENTRATE
Route Name ORAL
Start Marketing Date 20060101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Lannett Company, Inc.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


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