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Oxycodone HCl Controlled-Release - 63304-400-01 - (Oxycodone HCl Controlled-Release)

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Drug Information of Oxycodone HCl Controlled-Release

Product NDC: 63304-400
Proprietary Name: Oxycodone HCl Controlled-Release
Non Proprietary Name: Oxycodone HCl Controlled-Release
Active Ingredient(s): 10    mg/1 & nbsp;   Oxycodone HCl Controlled-Release
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone HCl Controlled-Release

Product NDC: 63304-400
Labeler Name: Ranbaxy Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020553
Marketing Category: NDA
Start Marketing Date: 20100201

Package Information of Oxycodone HCl Controlled-Release

Package NDC: 63304-400-01
Package Description: 100 TABLET in 1 BOTTLE (63304-400-01)

NDC Information of Oxycodone HCl Controlled-Release

NDC Code 63304-400-01
Proprietary Name Oxycodone HCl Controlled-Release
Package Description 100 TABLET in 1 BOTTLE (63304-400-01)
Product NDC 63304-400
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone HCl Controlled-Release
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name NDA
Labeler Name Ranbaxy Pharmaceuticals 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 HCl Controlled-Release


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