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Pentazocine Hydrochloride and Naloxone Hydrochloride - 43386-680-01 - (Pentazocine Hydrochloride and Naloxone Hydrochloride)

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Drug Information of Pentazocine Hydrochloride and Naloxone Hydrochloride

Product NDC: 43386-680
Proprietary Name: Pentazocine Hydrochloride and Naloxone Hydrochloride
Non Proprietary Name: Pentazocine Hydrochloride and Naloxone Hydrochloride
Active Ingredient(s): .5; 50    mg/1; mg/1 & nbsp;   Pentazocine Hydrochloride and Naloxone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pentazocine Hydrochloride and Naloxone Hydrochloride

Product NDC: 43386-680
Labeler Name: GAVIS Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075735
Marketing Category: ANDA
Start Marketing Date: 20110511

Package Information of Pentazocine Hydrochloride and Naloxone Hydrochloride

Package NDC: 43386-680-01
Package Description: 100 TABLET in 1 BOTTLE (43386-680-01)

NDC Information of Pentazocine Hydrochloride and Naloxone Hydrochloride

NDC Code 43386-680-01
Proprietary Name Pentazocine Hydrochloride and Naloxone Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (43386-680-01)
Product NDC 43386-680
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pentazocine Hydrochloride and Naloxone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110511
Marketing Category Name ANDA
Labeler Name GAVIS Pharmaceuticals, LLC
Substance Name NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE
Strength Number .5; 50
Strength Unit mg/1; mg/1
Pharmaceutical Classes Competitive Opioid Antagonists [MoA],Partial Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]

Complete Information of Pentazocine Hydrochloride and Naloxone Hydrochloride


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