Anectine - 0781-3009-95 - (Succinylcholine Chloride)

Alphabetical Index


Drug Information of Anectine

Product NDC: 0781-3009
Proprietary Name: Anectine
Non Proprietary Name: Succinylcholine Chloride
Active Ingredient(s): 20    mg/mL & nbsp;   Succinylcholine Chloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; PARENTERAL
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Anectine

Product NDC: 0781-3009
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008453
Marketing Category: NDA
Start Marketing Date: 19520820

Package Information of Anectine

Package NDC: 0781-3009-95
Package Description: 10 VIAL, MULTI-DOSE in 1 CARTON (0781-3009-95) > 10 mL in 1 VIAL, MULTI-DOSE (0781-3009-70)

NDC Information of Anectine

NDC Code 0781-3009-95
Proprietary Name Anectine
Package Description 10 VIAL, MULTI-DOSE in 1 CARTON (0781-3009-95) > 10 mL in 1 VIAL, MULTI-DOSE (0781-3009-70)
Product NDC 0781-3009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Succinylcholine Chloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; PARENTERAL
Start Marketing Date 19520820
Marketing Category Name NDA
Labeler Name Sandoz Inc
Substance Name SUCCINYLCHOLINE CHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Depolarizing Neuromuscular Blocker [EPC],Neuromuscular Depolarizing Blockade [PE]

Complete Information of Anectine


General Information