Quelicin - 0409-6629-61 - (Succinylcholine Chloride)

Alphabetical Index


Drug Information of Quelicin

Product NDC: 0409-6629
Proprietary Name: Quelicin
Non Proprietary Name: Succinylcholine Chloride
Active Ingredient(s): 20    mg/mL & nbsp;   Succinylcholine Chloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Quelicin

Product NDC: 0409-6629
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008845
Marketing Category: NDA
Start Marketing Date: 20100927

Package Information of Quelicin

Package NDC: 0409-6629-61
Package Description: 25 VIAL, MULTI-DOSE in 1 TRAY (0409-6629-61) > 10 mL in 1 VIAL, MULTI-DOSE

NDC Information of Quelicin

NDC Code 0409-6629-61
Proprietary Name Quelicin
Package Description 25 VIAL, MULTI-DOSE in 1 TRAY (0409-6629-61) > 10 mL in 1 VIAL, MULTI-DOSE
Product NDC 0409-6629
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Succinylcholine Chloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100927
Marketing Category Name NDA
Labeler Name Hospira, 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 Quelicin


General Information