FDA.reportPublic FDA data

Application 084364

Type
ANDA
Sponsor
WATSON LABS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001TRIHEXYPHENIDYL HYDROCHLORIDETRIHEXYPHENIDYL HYDROCHLORIDETABLET;ORAL5MGNoYes

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0591-5337Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideActavis Pharma, Inc.ANDACurrent
53808-0696Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideState of Florida DOH Central PharmacyANDACurrent
70518-1140Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1140Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1140Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1140Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1140Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1657Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1657Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1657Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1657Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent
70518-1657Trihexyphenidyl HydrochlorideTrihexyphenidyl HydrochlorideREMEDYREPACK INC.ANDACurrent