FDA.reportPublic FDA data

Succinylcholine Chloride

Product NDC
73043-021
11-digit product format
730430021
Labeler code
73043
Product ID
73043-021_69451f63-4c69-4774-a791-71257b8794ae
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Succinylcholine Chloride
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Devatis, Inc.
Application
ANDA214491
Marketing category
ANDA
Marketing start
2024-09-15
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

Additional Listing Data#

Finished product
Yes
Brand name base
Succinylcholine Chloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SUCCINYLCHOLINE CHLORIDE20 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiI9L0DDD30I
Rxcui1594589

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
abec1884-7093-4c95-8f57-c796012d60d8Product name220251120
810467f4-1d2b-8d95-dd9c-71dda6d03514Product name920250331

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73043-021-012023-11-15C16284748780-1f386c649-a3a7-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use SUCCINYLCHOLINE CHLORIDE INJECTION safely and effectively. See full prescribing information for SUCCINYLCHOLINE CHLORIDE INJECTION. SUCCINYLCHOLINE CHLORIDE injection, for intravenous or intramuscular use Initial U.S. Approval: 1952
73043-021-012023-01-30C16284748780-1f386c649-a3a7-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use SUCCINYLCHOLINE CHLORIDE INJECTION safely and effectively. See full prescribing information for SUCCINYLCHOLINE CHLORIDE INJECTION. SUCCINYLCHOLINE CHLORIDE injection, for intravenous or intramuscular use Initial U.S. Approval: 1952

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73043-021-01Succinylcholine Chloride10 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION1012
73043-021-01Succinylcholine Chloride25 in 1 CARTONINJECTION, SOLUTION2512

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73043-021SUCCINYLCHOLINE CHLORIDE INJECTION, SOLUTION [DEVATIS, INC.]12Current NDC, Legacy NDC, 2 package rows20241207_e235eb7d-5ce2-4884-9d16-493c90d7beba.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1594589succinylcholine chloride 20 MG/ML Injectable SolutionPSNe235eb7d-5ce2-4884-9d16-493c90d7beba12
1594589succinylcholine chloride 20 MG/ML Injectable SolutionSCDe235eb7d-5ce2-4884-9d16-493c90d7beba12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
73043-021-017304300210125 VIAL, MULTI-DOSE in 1 CARTON (73043-021-01) / 10 mL in 1 VIAL, MULTI-DOSE2024-09-150000-00-00NoNoCurrent