EXALGO - 23635-432-01 - (Hydromorphone Hydrochloride)

Alphabetical Index


Drug Information of EXALGO

Product NDC: 23635-432
Proprietary Name: EXALGO
Non Proprietary Name: Hydromorphone Hydrochloride
Active Ingredient(s): 32    mg/1 & nbsp;   Hydromorphone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of EXALGO

Product NDC: 23635-432
Labeler Name: Mallinckrodt, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021217
Marketing Category: NDA
Start Marketing Date: 20120824

Package Information of EXALGO

Package NDC: 23635-432-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23635-432-01)

NDC Information of EXALGO

NDC Code 23635-432-01
Proprietary Name EXALGO
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23635-432-01)
Product NDC 23635-432
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydromorphone Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120824
Marketing Category Name NDA
Labeler Name Mallinckrodt, Inc
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 32
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of EXALGO


General Information