FDA.reportPublic FDA data

Application 209285

Type
ANDA
Sponsor
LUPIN LTD

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001CLONIDINE HYDROCHLORIDECLONIDINE HYDROCHLORIDETABLET, EXTENDED RELEASE;ORAL0.1MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
68180-606Clonidine HydrochlorideClonidine HydrochlorideLupin Pharmaceuticals, Inc.ANDACurrent
68180-606Clonidine HydrochlorideClonidine HydrochlorideLupin Pharmaceuticals, Inc.ANDACurrent
68180-606Clonidine HydrochlorideClonidine HydrochlorideLupin Pharmaceuticals, Inc.ANDACurrent
68180-606Clonidine HydrochlorideClonidine HydrochlorideLupin Pharmaceuticals, Inc.ANDACurrent
68180-606Clonidine HydrochlorideClonidine HydrochlorideLupin Pharmaceuticals, Inc.ANDACurrent
70518-2110Clonidine HydrochlorideClonidine HydrochlorideREMEDYREPACK INC.ANDACurrent