Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 202852
Company: WATSON LABS INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription AT 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
11/24/2014 ORIG-1 Approval

Label is not available on this site.

DICLOFENAC SODIUM

SOLUTION;TOPICAL; 1.5%
TE Code = AT

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 206116 AMNEAL PHARMS
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 202027 APOTEX INC
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 204132 LUPIN LTD
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 205878 NOVEL LABS INC
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 203818 TARO
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 202769 TELIGENT PHARMA INC
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 202393 TWI PHARMS
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 202852 WATSON LABS INC
DICLOFENAC SODIUM DICLOFENAC SODIUM 1.5% SOLUTION;TOPICAL Prescription No AT 206411 ZYDUS PHARMS

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