Regonol - 0781-3040-95 - (Pyridostigmine Bromide)

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Drug Information of Regonol

Product NDC: 0781-3040
Proprietary Name: Regonol
Non Proprietary Name: Pyridostigmine Bromide
Active Ingredient(s): 5    mg/mL & nbsp;   Pyridostigmine Bromide
Administration Route(s): INTRAVENOUS; PARENTERAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Regonol

Product NDC: 0781-3040
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017398
Marketing Category: NDA
Start Marketing Date: 20050510

Package Information of Regonol

Package NDC: 0781-3040-95
Package Description: 10 AMPULE in 1 CARTON (0781-3040-95) > 2 mL in 1 AMPULE (0781-3040-72)

NDC Information of Regonol

NDC Code 0781-3040-95
Proprietary Name Regonol
Package Description 10 AMPULE in 1 CARTON (0781-3040-95) > 2 mL in 1 AMPULE (0781-3040-72)
Product NDC 0781-3040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pyridostigmine Bromide
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; PARENTERAL
Start Marketing Date 20050510
Marketing Category Name NDA
Labeler Name Sandoz Inc
Substance Name PYRIDOSTIGMINE BROMIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Regonol


General Information