FDA.reportPublic FDA data

Succinylcholine Chloride

Product NDC
70710-1377
11-digit product format
707101377
Labeler code
70710
Product ID
70710-1377_bd190da3-9daf-4859-a431-87c693e18e90
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Succinylcholine Chloride
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Zydus Pharmaceuticals USA Inc.
Application
ANDA209467
Marketing category
ANDA
Marketing start
2018-05-10
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
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-1377-1Succinylcholine Chloride10 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION109
70710-1377-2Succinylcholine Chloride25 in 1 TRAYINJECTION, SOLUTION259

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70710-1377-1ML - Milliliter70710-13770650a30e-e9da-4f34-bf4f-5cacc2bbe06612018-08-13
70710-1377-2ML - Milliliter70710-1377044a00b1-4fe9-48a2-91e7-78853f08882d12018-08-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70710-1377SUCCINYLCHOLINE CHLORIDE INJECTION, SOLUTION [ZYDUS PHARMACEUTICALS USA INC.]9Current NDC, Legacy NDC, 2 package rows20230107_017e5ad4-028e-4e34-ac09-d0c8d64c880a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1594589succinylcholine chloride 20 MG/ML Injectable SolutionPSN017e5ad4-028e-4e34-ac09-d0c8d64c880a9
1594589succinylcholine chloride 20 MG/ML Injectable SolutionSCD017e5ad4-028e-4e34-ac09-d0c8d64c880a9

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70710-1377-17071013770110 mL in 1 VIAL, MULTI-DOSE10 mlHistorical
70710-1377-27071013770225 VIAL, MULTI-DOSE in 1 TRAY (70710-1377-2) / 10 mL in 1 VIAL, MULTI-DOSE (70710-1377-1) 2018-05-100000-00-00NoNoCurrent