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Nalbuphine Hydrochloride - 63739-466-05 - (Nalbuphine Hydrochloride)

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Drug Information of Nalbuphine Hydrochloride

Product NDC: 63739-466
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: 63739-466
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070916
Marketing Category: ANDA
Start Marketing Date: 20100503

Package Information of Nalbuphine Hydrochloride

Package NDC: 63739-466-05
Package Description: 5 POUCH in 1 BOX (63739-466-05) > 1 AMPULE in 1 POUCH (63739-466-21) > 1 mL in 1 AMPULE

NDC Information of Nalbuphine Hydrochloride

NDC Code 63739-466-05
Proprietary Name Nalbuphine Hydrochloride
Package Description 5 POUCH in 1 BOX (63739-466-05) > 1 AMPULE in 1 POUCH (63739-466-21) > 1 mL in 1 AMPULE
Product NDC 63739-466
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nalbuphine Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20100503
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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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