Application 090134

Type
ANDA
Sponsor
ACTAVIS ELIZABETH

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DOXYCYCLINE HYCLATEDOXYCYCLINE HYCLATETABLET, DELAYED RELEASE;ORALEQ 75MG BASENoNo
002DOXYCYCLINE HYCLATEDOXYCYCLINE HYCLATETABLET, DELAYED RELEASE;ORALEQ 100MG BASENoNo
003DOXYCYCLINE HYCLATEDOXYCYCLINE HYCLATETABLET, DELAYED RELEASE;ORALEQ 50MG BASENoNo
004DOXYCYCLINE HYCLATEDOXYCYCLINE HYCLATETABLET, DELAYED RELEASE;ORALEQ 200MG BASENoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0591-4550Doxycycline HyclateDoxycycline HyclateActavis Pharma, Inc.ANDACurrent
0591-4550Doxycycline HyclateDoxycycline HyclateActavis Pharma, Inc.ANDACurrent
0591-4550Doxycycline HyclateDoxycycline HyclateActavis Pharma, Inc.ANDACurrent
0591-4575Doxycycline HyclateDoxycycline HyclateActavis Pharma, Inc.ANDACurrent
0591-4575Doxycycline HyclateDoxycycline HyclateActavis Pharma, Inc.ANDACurrent
0591-4575Doxycycline HyclateDoxycycline HyclateActavis Pharma, Inc.ANDACurrent

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
54007SUPPL2018-05-03