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Hydromorphone Hydrochloride - 54868-3165-6 - (Hydromorphone Hydrochloride)

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Drug Information of Hydromorphone Hydrochloride

Product NDC: 54868-3165
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Hydromorphone Hydrochloride

Product NDC: 54868-3165
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078273
Marketing Category: ANDA
Start Marketing Date: 20040920

Package Information of Hydromorphone Hydrochloride

Package NDC: 54868-3165-6
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE (54868-3165-6)

NDC Information of Hydromorphone Hydrochloride

NDC Code 54868-3165-6
Proprietary Name Hydromorphone Hydrochloride
Package Description 120 TABLET, FILM COATED in 1 BOTTLE (54868-3165-6)
Product NDC 54868-3165
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydromorphone Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040920
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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