Home > National Drug Code (NDC) > Rocuronium Bromide

Rocuronium Bromide - 0781-3220-70 - (Rocuronium Bromide)

Alphabetical Index


Drug Information of Rocuronium Bromide

Product NDC: 0781-3220
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, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rocuronium Bromide

Product NDC: 0781-3220
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079195
Marketing Category: ANDA
Start Marketing Date: 20081205

Package Information of Rocuronium Bromide

Package NDC: 0781-3220-70
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3220-70) > 10 mL in 1 VIAL, MULTI-DOSE

NDC Information of Rocuronium Bromide

NDC Code 0781-3220-70
Proprietary Name Rocuronium Bromide
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3220-70) > 10 mL in 1 VIAL, MULTI-DOSE
Product NDC 0781-3220
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rocuronium Bromide
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20081205
Marketing Category Name ANDA
Labeler Name Sandoz 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


General Information