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Nalbuphine Hydrochloride - 0409-1467-01 - (NALBUPHINE HYDROCHLORIDE)

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Drug Information of Nalbuphine Hydrochloride

Product NDC: 0409-1467
Proprietary Name: Nalbuphine Hydrochloride
Non Proprietary Name: NALBUPHINE HYDROCHLORIDE
Active Ingredient(s): 20    mg/mL & nbsp;   NALBUPHINE HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nalbuphine Hydrochloride

Product NDC: 0409-1467
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070918
Marketing Category: ANDA
Start Marketing Date: 20110822

Package Information of Nalbuphine Hydrochloride

Package NDC: 0409-1467-01
Package Description: 25 VIAL, MULTI-DOSE in 1 CARTON (0409-1467-01) > 10 mL in 1 VIAL, MULTI-DOSE

NDC Information of Nalbuphine Hydrochloride

NDC Code 0409-1467-01
Proprietary Name Nalbuphine Hydrochloride
Package Description 25 VIAL, MULTI-DOSE in 1 CARTON (0409-1467-01) > 10 mL in 1 VIAL, MULTI-DOSE
Product NDC 0409-1467
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NALBUPHINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20110822
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name NALBUPHINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Competitive Opioid Antagonists [MoA],Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA]

Complete Information of Nalbuphine Hydrochloride


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