FDA.reportPublic FDA data

Application 211589

Type
ANDA
Sponsor
SOMERSET THERAPS LLC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001SUCCINYLCHOLINE CHLORIDESUCCINYLCHOLINE CHLORIDEINJECTABLE;INJECTION20MG/MLNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
70069-301Succinylcholine ChlorideSuccinylcholine ChlorideSomerset Therapeutics, LLCANDACurrent
70069-301Succinylcholine ChlorideSuccinylcholine ChlorideSomerset Therapeutics, LLCANDACurrent
70069-301Succinylcholine ChlorideSuccinylcholine ChlorideSomerset Therapeutics, LLCANDACurrent
70069-301Succinylcholine ChlorideSuccinylcholine ChlorideSomerset Therapeutics, LLCANDACurrent
71872-7221Succinylcholine ChlorideSuccinylcholine ChlorideMedical Purchasing Solutions, LLCANDACurrent