FDA.reportPublic FDA data

Application 216003

Type
ANDA
Sponsor
BE PHARMS

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
71839-121Succinylcholine ChlorideSuccinylcholine ChlorideBE Pharmaceuticals Inc.ANDACurrent
71839-121Succinylcholine ChlorideSuccinylcholine ChlorideBE Pharmaceuticals Inc.ANDACurrent