Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 209106
Company: LUPIN LTD
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE OINTMENT, AUGMENTED;TOPICAL Prescription AB No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
12/18/2019 ORIG-1 Approval STANDARD

Label is not available on this site.

BETAMETHASONE DIPROPIONATE

OINTMENT, AUGMENTED;TOPICAL; EQ 0.05% BASE
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE OINTMENT, AUGMENTED;TOPICAL Prescription No AB 074304 ACTAVIS MID ATLANTIC
BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE OINTMENT, AUGMENTED;TOPICAL Prescription No AB 075373 FOUGERA PHARMS
BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE OINTMENT, AUGMENTED;TOPICAL Prescription No AB 209106 LUPIN LTD
BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE OINTMENT, AUGMENTED;TOPICAL Prescription No AB 076753 TARO
BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE OINTMENT, AUGMENTED;TOPICAL Prescription No AB 206118 TELIGENT
DIPROLENE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE OINTMENT, AUGMENTED;TOPICAL Prescription Yes AB 018741 MERCK SHARP DOHME

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