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Dilaudid HP - 59011-446-25 - (hydromorphone hydrochloride)

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Drug Information of Dilaudid HP

Product NDC: 59011-446
Proprietary Name: Dilaudid HP
Non Proprietary Name: hydromorphone hydrochloride
Active Ingredient(s): 10    mg/mL & nbsp;   hydromorphone hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dilaudid HP

Product NDC: 59011-446
Labeler Name: Purdue Pharma LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019034
Marketing Category: NDA
Start Marketing Date: 19840111

Package Information of Dilaudid HP

Package NDC: 59011-446-25
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON (59011-446-25) > 25 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Dilaudid HP

NDC Code 59011-446-25
Proprietary Name Dilaudid HP
Package Description 1 VIAL, SINGLE-DOSE in 1 CARTON (59011-446-25) > 25 mL in 1 VIAL, SINGLE-DOSE
Product NDC 59011-446
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydromorphone hydrochloride
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19840111
Marketing Category Name NDA
Labeler Name Purdue Pharma LP
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Dilaudid HP


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