FDA.report

Application 206581

Type
ANDA
Sponsor
PERRIGO R AND D

Related Records

Application Products

ProductDrugIngredientFormStrengthReference drugReference standard
001IBUPROFEN SODIUMIBUPROFEN SODIUMTABLET;ORALEQ 200MG BASENoNo

NDC Listings For This Application

NDCNameNonproprietary nameLabelerMarketing categoryStatus
0363-0909Ibuprofen SodiumIbuprofenWalgreen CompanyANDACurrent
0363-0909Ibuprofen SodiumIbuprofenWalgreen CompanyANDACurrent
11673-835Up and Up Ibuprofen SodiumIbuprofenTarget CorporationANDACurrent
11673-835Up and Up Ibuprofen SodiumIbuprofenTarget CorporationANDACurrent
36800-303Topcare IbuprofenIbuprofenTopco Associates LLCANDACurrent
36800-303Topcare IbuprofenIbuprofenTopco Associates LLCANDACurrent
41250-920IbuprofenIbuprofenMeijer Distribution IncANDACurrent
41250-920IbuprofenIbuprofenMeijer Distribution IncANDACurrent
46122-341Good Neighbor Pharmacy IbuprofenIbuprofenAmerisource BergenANDACurrent
46122-341Good Neighbor Pharmacy IbuprofenIbuprofenAmerisource BergenANDACurrent
69842-709ibuprofenIbuprofenCVS PharmacyANDACurrent
69842-709ibuprofenIbuprofenCVS PharmacyANDACurrent
69842-835CVS Ibuprofen SodiumIbuprofenCVS PharmacyANDACurrent
69842-835CVS Ibuprofen SodiumIbuprofenCVS PharmacyANDACurrent

Documents

DocumentTitleSubmission typeSubmission no.DateStorage
328160ORIG12015-08-06Cached in FDA.report object storage
197260ORIG12015-08-06Cached in FDA.report object storage