Nimbex - 0074-4382-20 - (Cisatracurium besylate)

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Drug Information of Nimbex

Product NDC: 0074-4382
Proprietary Name: Nimbex
Non Proprietary Name: Cisatracurium besylate
Active Ingredient(s): 10    mg/mL & nbsp;   Cisatracurium besylate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nimbex

Product NDC: 0074-4382
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020551
Marketing Category: NDA
Start Marketing Date: 19951215

Package Information of Nimbex

Package NDC: 0074-4382-20
Package Description: 20 mL in 1 VIAL, SINGLE-DOSE (0074-4382-20)

NDC Information of Nimbex

NDC Code 0074-4382-20
Proprietary Name Nimbex
Package Description 20 mL in 1 VIAL, SINGLE-DOSE (0074-4382-20)
Product NDC 0074-4382
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cisatracurium besylate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19951215
Marketing Category Name NDA
Labeler Name Abbott Laboratories
Substance Name CISATRACURIUM BESYLATE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]

Complete Information of Nimbex


General Information