Lovastatin tablet

Information for patients

Patients should be advised about substances they should not take concomitantly with lovastatin and be advised to report promptly unexplained muscle pain, tenderness, or weakness (see list below and WARNINGS, Myopathy/Rhabdomyolysis). Patients should also be advised to inform other physicians prescribing a new medication that they are taking lovastatin.

Ingredients and appearance - Product information

Lovastatin tablet- Lovastatin

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 49349-531
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Lovastatin ( UNII: 9LHU78OQFD)( Lovastatin - UNII: 9LHU78OQFD ) 40 mgin 1

Inactive Ingredients

Ingredient Name Code
Lactose monohydrate ( UNII: EWQ57Q8I5X)
Magnesium stearate ( UNII: 70097M6I30)
Cellulose, microcrystalline ( UNII: OP1R32D61U)
Starch, corn ( UNII: O8232NY3SJ)
Butylated hydroxyanisole ( UNII: REK4960K2U)

Product Characteristics

Color yellow Score 1
Shape ROUND (TABLET) Imprint Code 635
Size 8 mm


# Item Code Package Description Marketing Start Date
1 NDC: 49349-531-02 30 in 1 BLISTER PACK 2011/09/23

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA075828 USA 2011/09/23

Labeler - REMEDYREPACK INC.( 829572556)