FDA.reportPublic FDA data

Application 065171

Type
ANDA
Sponsor
BARR

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DEMECLOCYCLINE HYDROCHLORIDEDEMECLOCYCLINE HYDROCHLORIDETABLET;ORAL150MGNoNo
002DEMECLOCYCLINE HYDROCHLORIDEDEMECLOCYCLINE HYDROCHLORIDETABLET;ORAL300MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0555-0701Demeclocycline HydrochlorideDemeclocycline HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0701Demeclocycline HydrochlorideDemeclocycline HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0701Demeclocycline HydrochlorideDemeclocycline HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0702Demeclocycline HydrochlorideDemeclocycline HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0702Demeclocycline HydrochlorideDemeclocycline HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-0702Demeclocycline HydrochlorideDemeclocycline HydrochlorideTeva Pharmaceuticals USA, Inc.ANDACurrent