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Hydromorphone Hydrochloride - 0409-2634-01 - (HYDROMORPHONE HYDROCHLORIDE)

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Drug Information of Hydromorphone Hydrochloride

Product NDC: 0409-2634
Proprietary Name: Hydromorphone Hydrochloride
Non Proprietary Name: HYDROMORPHONE HYDROCHLORIDE
Active Ingredient(s): 10    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 Hydromorphone Hydrochloride

Product NDC: 0409-2634
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078591
Marketing Category: ANDA
Start Marketing Date: 20100819

Package Information of Hydromorphone Hydrochloride

Package NDC: 0409-2634-01
Package Description: 10 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-01) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Hydromorphone Hydrochloride

NDC Code 0409-2634-01
Proprietary Name Hydromorphone Hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-01) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-2634
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROMORPHONE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20100819
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
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


General Information