Home > National Drug Code (NDC) > HYDROMORPHONE HYDROCHLORIDE

HYDROMORPHONE HYDROCHLORIDE - 10544-374-08 - (HYDROMORPHONE HYDROCHLORIDE)

Alphabetical Index


Drug Information of HYDROMORPHONE HYDROCHLORIDE

Product NDC: 10544-374
Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
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 HYDROMORPHONE HYDROCHLORIDE

Product NDC: 10544-374
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078273
Marketing Category: ANDA
Start Marketing Date: 20080529

Package Information of HYDROMORPHONE HYDROCHLORIDE

Package NDC: 10544-374-08
Package Description: 168 TABLET in 1 BOTTLE (10544-374-08)

NDC Information of HYDROMORPHONE HYDROCHLORIDE

NDC Code 10544-374-08
Proprietary Name HYDROMORPHONE HYDROCHLORIDE
Package Description 168 TABLET in 1 BOTTLE (10544-374-08)
Product NDC 10544-374
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROMORPHONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080529
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of HYDROMORPHONE HYDROCHLORIDE


General Information