Leader all day pain relief tablet, film coated

Ingredients and appearance - Product information

Leader all day pain relief tablet, film coated- Naproxen sodium

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 37205-262
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Naproxen sodium ( UNII: 9TN87S3A3C)( Naproxen - UNII: 57Y76R9ATQ ) 220 mgin 1

Inactive Ingredients

Ingredient Name Code
Croscarmellose sodium ( UNII: M28OL1HH48)
Fd&c blue no. 2 ( UNII: L06K8R7DQK)
Polyethylene glycol 1000 ( UNII: U076Q6Q621)
Magnesium stearate ( UNII: 70097M6I30)
Polyvinyl alcohol ( UNII: 532B59J990)
Povidones ( UNII: FZ989GH94E)
Talc ( UNII: 7SEV7J4R1U)
Titanium dioxide ( UNII: 15FIX9V2JP)

Product Characteristics

Color BLUE (Light Blue) Imprint Code I3
Score 1 Shape CAPSULE (oval)
Size 12 mm

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA079096 USA

Labeler - Cardinal Health (Leader) 37205( 097537435)