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Hydromorphone Hydrochloride - 17478-540-05 - (Hydromorphone Hydrochloride)

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Drug Information of Hydromorphone Hydrochloride

Product NDC: 17478-540
Proprietary Name: Hydromorphone Hydrochloride
Non Proprietary Name: Hydromorphone Hydrochloride
Active Ingredient(s): 10    mg/mL & nbsp;   Hydromorphone Hydrochloride
Administration Route(s): PARENTERAL
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydromorphone Hydrochloride

Product NDC: 17478-540
Labeler Name: Akorn
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078228
Marketing Category: ANDA
Start Marketing Date: 20100515

Package Information of Hydromorphone Hydrochloride

Package NDC: 17478-540-05
Package Description: 10 AMPULE in 1 CARTON (17478-540-05) > 5 mL in 1 AMPULE

NDC Information of Hydromorphone Hydrochloride

NDC Code 17478-540-05
Proprietary Name Hydromorphone Hydrochloride
Package Description 10 AMPULE in 1 CARTON (17478-540-05) > 5 mL in 1 AMPULE
Product NDC 17478-540
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydromorphone Hydrochloride
Dosage Form Name INJECTION
Route Name PARENTERAL
Start Marketing Date 20100515
Marketing Category Name ANDA
Labeler Name Akorn
Substance Name HYDROMORPHONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Hydromorphone Hydrochloride


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