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Atracurium Besylate - 55390-103-10 - (Atracurium Besylate)

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Drug Information of Atracurium Besylate

Product NDC: 55390-103
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
Coding System: National Drug Codes(NDC)

Labeler Information of Atracurium Besylate

Product NDC: 55390-103
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074901
Marketing Category: ANDA
Start Marketing Date: 19970915

Package Information of Atracurium Besylate

Package NDC: 55390-103-10
Package Description: 10 VIAL in 1 BOX (55390-103-10) > 10 mL in 1 VIAL

NDC Information of Atracurium Besylate

NDC Code 55390-103-10
Proprietary Name Atracurium Besylate
Package Description 10 VIAL in 1 BOX (55390-103-10) > 10 mL in 1 VIAL
Product NDC 55390-103
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Atracurium Besylate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19970915
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
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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