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Diclofenac PotassiumDrug - Diclofenac Potassium The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Diclofenac Potassium
Strength -
50MG
Applicant -
WATSON LABS
New Drug Application (NDA) Number -
075152
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Nov 27, 1998
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Watson Laboratories Inc
Diclofenac Potassium
Cataflam 50mg Tablet; Oral
Diclofenac Potassium 50mg Tablet; Oral Diclofenac Potassium 50mg Tablet; Oral Diclofenac Potassium 50mg Tablet; Oral Diclofenac Potassium 50mg Tablet; Oral Diclofenac Potassium 50mg Tablet; Oral Diclofenac Potassium 50mg Tablet; Oral Diclofenac Potassium 50mg Tablet; Oral Daranide 50mg Tablet; Oral Cataflam 25mg **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Tablet; Oral NewDrugInformation |