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Atracurium Besylate - 0409-1109-01 - (ATRACURIUM BESYLATE)

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Drug Information of Atracurium Besylate

Product NDC: 0409-1109
Proprietary Name: Atracurium Besylate
Non Proprietary Name: ATRACURIUM BESYLATE
Active Ingredient(s): 10    mg/mL & nbsp;   ATRACURIUM BESYLATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Atracurium Besylate

Product NDC: 0409-1109
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090782
Marketing Category: ANDA
Start Marketing Date: 20121018

Package Information of Atracurium Besylate

Package NDC: 0409-1109-01
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1109-01) > 5 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Atracurium Besylate

NDC Code 0409-1109-01
Proprietary Name Atracurium Besylate
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1109-01) > 5 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-1109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ATRACURIUM BESYLATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20121018
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name ATRACURIUM BESYLATE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]

Complete Information of Atracurium Besylate


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