Label: IVERMECTIN tablet
- NDC Code(s): 70771-1731-2, 70771-1731-3
- Packager: Zydus Lifesciences Limited
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated February 27, 2026
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- SPL UNCLASSIFIED SECTION
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INGREDIENTS AND APPEARANCE
IVERMECTIN
ivermectin tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70771-1731 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IVERMECTIN (UNII: 8883YP2R6D) (IVERMECTIN - UNII:8883YP2R6D) IVERMECTIN 3 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) FERRIC OXIDE RED (UNII: 1K09F3G675) HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color RED (Red to brown) Score no score Shape ROUND Size 5mm Flavor Imprint Code 1771 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70771-1731-3 2 in 1 CARTON 02/27/2026 1 NDC:70771-1731-2 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA216863 02/27/2026 Labeler - Zydus Lifesciences Limited (918596198)
