Levothyroxine sodium tablet

Ingredients and appearance - Product information

Levothyroxine sodium tablet- Levothyroxine sodium

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 50436-4380
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Levothyroxine sodium ( UNII: 9J765S329G)( Levothyroxine - UNII: Q51BO43MG4 ) 0.15 mgin 1

Inactive Ingredients

Ingredient Name Code
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Lactose ( UNII: J2B2A4N98G)
Magnesium stearate ( UNII: 70097M6I30)
Cellulose, microcrystalline ( UNII: OP1R32D61U)
Starch, corn ( UNII: O8232NY3SJ)
Acacia ( UNII: 5C5403N26O)
Sodium starch glycolate type a potato ( UNII: 5856J3G2A2)
Fd&c blue no. 2 ( UNII: L06K8R7DQK)
Aluminum oxide ( UNII: LMI26O6933)

Product Characteristics

Color BLUE (Light Blue) Imprint Code JSP;520
Score 2 Shape ROUND
Size 7 mm

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 50436-4380-1 90 in 1 BOTTLE 2003/12/01
2 NDC: 50436-4380-2 30 in 1 BOTTLE 2003/12/01

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
NDA NDA021210 USA 2003/12/01

Labeler - Unit Dose Services( 831995316)

Establishment

Name ID/FEI Business Operations
Unit Dose Services 831995316 REPACK( 50436-4380)

Levothyroxine sodium tablet