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Pentazocine and naloxone - 68387-531-30 - (PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE)

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Drug Information of Pentazocine and naloxone

Product NDC: 68387-531
Proprietary Name: Pentazocine and naloxone
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 and naloxone

Product NDC: 68387-531
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074736
Marketing Category: ANDA
Start Marketing Date: 20090721

Package Information of Pentazocine and naloxone

Package NDC: 68387-531-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (68387-531-30)

NDC Information of Pentazocine and naloxone

NDC Code 68387-531-30
Proprietary Name Pentazocine and naloxone
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (68387-531-30)
Product NDC 68387-531
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090721
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
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 and naloxone


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