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OxaprozinDrug - Oxaprozin The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Oxaprozin
Strength -
600MG
Applicant -
APOTEX
New Drug Application (NDA) Number -
075987
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Sep 2, 2004
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Apotex Inc
Oxaprozin
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