Nabumetone tablet, film coated

Ingredients and appearance - Product information

Nabumetone tablet, film coated- Nabumetone

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 68788-7220
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Nabumetone ( UNII: LW0TIW155Z)( Nabumetone - UNII: LW0TIW155Z ) 500 mgin 1

Inactive Ingredients

Ingredient Name Code
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Starch, corn ( UNII: O8232NY3SJ)
Hypromellose, unspecified ( UNII: 3NXW29V3WO)
Magnesium stearate ( UNII: 70097M6I30)
Povidone, unspecified ( UNII: FZ989GH94E)
Sodium lauryl sulfate ( UNII: 368GB5141J)
Sodium starch glycolate type a potato ( UNII: 5856J3G2A2)
Titanium dioxide ( UNII: 15FIX9V2JP)
Triacetin ( UNII: XHX3C3X673)
Talc ( UNII: 7SEV7J4R1U)

Product Characteristics

Color WHITE Size 17 mm
Shape OVAL Score 1
Imprint Code 3670

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA091083 USA

Labeler - Preferred Pharmaceuticals Inc.( 791119022)

Establishment

Name ID/FEI Business Operations
Preferred Pharmaceuticals Inc. 791119022 REPACK( 68788-7220)