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NabumetoneDrug - Nabumetone The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Nabumetone
Strength -
500MG
Applicant -
SANDOZ
New Drug Application (NDA) Number -
075590
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Feb 25, 2002
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Sandoz Inc
Nabumetone
Nabumetone 750mg Tablet; Oral
Nabumetone 500mg Tablet; Oral Nabumetone 500mg Tablet; Oral Cellcept 500mg Tablet; Oral Cellcept 500mg/vial Injectable; Injection Myfortic 180mg Tablet, Delayed Release; Oral Myfortic 360mg Tablet, Delayed Release; Oral Cesamet 1mg Capsule; Oral Nabumetone 750mg Tablet; Oral Nabumetone 500mg Tablet; Oral NewDrugInformation |