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Rocuronium Bromide - 10139-235-11 - (rocuronium bromide)

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Drug Information of Rocuronium Bromide

Product NDC: 10139-235
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): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rocuronium Bromide

Product NDC: 10139-235
Labeler Name: GeneraMedix Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079199
Marketing Category: ANDA
Start Marketing Date: 20120118

Package Information of Rocuronium Bromide

Package NDC: 10139-235-11
Package Description: 10 VIAL, MULTI-DOSE in 1 CARTON (10139-235-11) > 10 mL in 1 VIAL, MULTI-DOSE

NDC Information of Rocuronium Bromide

NDC Code 10139-235-11
Proprietary Name Rocuronium Bromide
Package Description 10 VIAL, MULTI-DOSE in 1 CARTON (10139-235-11) > 10 mL in 1 VIAL, MULTI-DOSE
Product NDC 10139-235
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rocuronium bromide
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20120118
Marketing Category Name ANDA
Labeler Name GeneraMedix 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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