Application 090358

Type
ANDA
Sponsor
SUN PHARM

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001SUMATRIPTAN SUCCINATESUMATRIPTAN SUCCINATEINJECTABLE;SUBCUTANEOUSEQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)NoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
47335-276Sumatriptan SuccinateSumatriptan SuccinateSun Pharmaceutical Industries, Inc.ANDACurrent
47335-276Sumatriptan SuccinateSumatriptan SuccinateSun Pharmaceutical Industries, Inc.ANDACurrent

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
43237ORIG2013-09-09