Dilaudid - 54868-2905-1 - (hydromorphone hydrochloride)

Alphabetical Index


Drug Information of Dilaudid

Product NDC: 54868-2905
Proprietary Name: Dilaudid
Non Proprietary Name: hydromorphone hydrochloride
Active Ingredient(s): 4    mg/1 & nbsp;   hydromorphone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dilaudid

Product NDC: 54868-2905
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019892
Marketing Category: NDA
Start Marketing Date: 20041011

Package Information of Dilaudid

Package NDC: 54868-2905-1
Package Description: 100 TABLET in 1 BOTTLE (54868-2905-1)

NDC Information of Dilaudid

NDC Code 54868-2905-1
Proprietary Name Dilaudid
Package Description 100 TABLET in 1 BOTTLE (54868-2905-1)
Product NDC 54868-2905
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydromorphone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041011
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Dilaudid


General Information