Dilaudid - 59011-444-10 - (hydromorphone hydrochloride)

Alphabetical Index


Drug Information of Dilaudid

Product NDC: 59011-444
Proprietary Name: Dilaudid
Non Proprietary Name: hydromorphone hydrochloride
Active Ingredient(s): 4    mg/mL & nbsp;   hydromorphone hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dilaudid

Product NDC: 59011-444
Labeler Name: Purdue Pharma LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019034
Marketing Category: NDA
Start Marketing Date: 19260101

Package Information of Dilaudid

Package NDC: 59011-444-10
Package Description: 10 AMPULE in 1 CARTON (59011-444-10) > 4 mL in 1 AMPULE

NDC Information of Dilaudid

NDC Code 59011-444-10
Proprietary Name Dilaudid
Package Description 10 AMPULE in 1 CARTON (59011-444-10) > 4 mL in 1 AMPULE
Product NDC 59011-444
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydromorphone hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19260101
Marketing Category Name NDA
Labeler Name Purdue Pharma LP
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Dilaudid


General Information