FDA.reportPublic FDA data

Application 074672

Type
ANDA
Sponsor
MLV

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001SELEGILINE HYDROCHLORIDESELEGILINE HYDROCHLORIDETABLET;ORAL5MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
72319-006Selegiline HydrochlorideSelegiline Hydrochloridei3 Pharmaceuticals, LLCANDACurrent
72319-006Selegiline HydrochlorideSelegiline Hydrochloridei3 Pharmaceuticals, LLCANDACurrent
72319-006Selegiline HydrochlorideSelegiline Hydrochloridei3 Pharmaceuticals, LLCANDACurrent