Succinylcholine Chloride

Product NDC
71872-7272
11-digit product format
718727272
Labeler code
71872
Product ID
71872-7272_facbeb60-fce4-d11a-e053-6294a90aafaf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Succinylcholine Chloride
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Medical Purchasing Solutions, LLC
Application
ANDA213810
Marketing category
ANDA
Marketing start
2020-05-04
Substance
SUCCINYLCHOLINE CHLORIDE
Active strength
20 mg/mL
Pharmacologic classes
Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
I9L0DDD30ISUCCINYLCHOLINE CHLORIDE71-27-2SUCCINYLCHOLINE CHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71872-7272-1718727272011 VIAL, MULTI-DOSE in 1 BAG (71872-7272-1) / 10 mL in 1 VIAL, MULTI-DOSE2021-11-30NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Succinylcholine ChlorideMedical Purchasing Solutions, LLC2023-05-03HUMAN PRESCRIPTION DRUG LABEL2