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Hydromorphone Hydrochloride - 63629-4284-8 - (Hydromorphone Hydrochloride)

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Drug Information of Hydromorphone Hydrochloride

Product NDC: 63629-4284
Proprietary Name: Hydromorphone Hydrochloride
Non Proprietary Name: Hydromorphone Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Hydromorphone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydromorphone Hydrochloride

Product NDC: 63629-4284
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019892
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20091123

Package Information of Hydromorphone Hydrochloride

Package NDC: 63629-4284-8
Package Description: 20 TABLET in 1 BOTTLE (63629-4284-8)

NDC Information of Hydromorphone Hydrochloride

NDC Code 63629-4284-8
Proprietary Name Hydromorphone Hydrochloride
Package Description 20 TABLET in 1 BOTTLE (63629-4284-8)
Product NDC 63629-4284
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydromorphone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091123
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Bryant Ranch Prepack
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Hydromorphone Hydrochloride


General Information