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cisatracurium besylate - 0781-9037-95 - (cisatracurium besylate)

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Drug Information of cisatracurium besylate

Product NDC: 0781-9037
Proprietary Name: cisatracurium besylate
Non Proprietary Name: cisatracurium besylate
Active Ingredient(s): 2    mg/mL & nbsp;   cisatracurium besylate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of cisatracurium besylate

Product NDC: 0781-9037
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200154
Marketing Category: ANDA
Start Marketing Date: 20130228

Package Information of cisatracurium besylate

Package NDC: 0781-9037-95
Package Description: 10 VIAL in 1 CARTON (0781-9037-95) > 5 mL in 1 VIAL

NDC Information of cisatracurium besylate

NDC Code 0781-9037-95
Proprietary Name cisatracurium besylate
Package Description 10 VIAL in 1 CARTON (0781-9037-95) > 5 mL in 1 VIAL
Product NDC 0781-9037
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cisatracurium besylate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20130228
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CISATRACURIUM BESYLATE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]

Complete Information of cisatracurium besylate


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