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Butorphanol Tartrate - 55390-344-01 - (Butorphanol Tartrate)

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Drug Information of Butorphanol Tartrate

Product NDC: 55390-344
Proprietary Name: Butorphanol Tartrate
Non Proprietary Name: Butorphanol Tartrate
Active Ingredient(s): 2    mg/mL & nbsp;   Butorphanol Tartrate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Butorphanol Tartrate

Product NDC: 55390-344
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075046
Marketing Category: ANDA
Start Marketing Date: 20080505

Package Information of Butorphanol Tartrate

Package NDC: 55390-344-01
Package Description: 1 VIAL in 1 BOX (55390-344-01) > 10 mL in 1 VIAL

NDC Information of Butorphanol Tartrate

NDC Code 55390-344-01
Proprietary Name Butorphanol Tartrate
Package Description 1 VIAL in 1 BOX (55390-344-01) > 10 mL in 1 VIAL
Product NDC 55390-344
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Butorphanol Tartrate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080505
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name BUTORPHANOL TARTRATE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Competitive Opioid Antagonists [MoA],Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA]

Complete Information of Butorphanol Tartrate


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