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rocuronium bromide - 39822-4200-6 - (rocuronium bromide)

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Drug Information of rocuronium bromide

Product NDC: 39822-4200
Proprietary Name: rocuronium bromide
Non Proprietary Name: rocuronium bromide
Active Ingredient(s): 10    mg/mL & nbsp;   rocuronium bromide
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of rocuronium bromide

Product NDC: 39822-4200
Labeler Name: X-GEN Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091115
Marketing Category: ANDA
Start Marketing Date: 20121201

Package Information of rocuronium bromide

Package NDC: 39822-4200-6
Package Description: 10 VIAL in 1 CARTON (39822-4200-6) > 10 mL in 1 VIAL (39822-4200-5)

NDC Information of rocuronium bromide

NDC Code 39822-4200-6
Proprietary Name rocuronium bromide
Package Description 10 VIAL in 1 CARTON (39822-4200-6) > 10 mL in 1 VIAL (39822-4200-5)
Product NDC 39822-4200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rocuronium bromide
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20121201
Marketing Category Name ANDA
Labeler Name X-GEN Pharmaceuticals, Inc.
Substance Name ROCURONIUM BROMIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC]

Complete Information of rocuronium bromide


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