NDC 70771-1731 – Ivermectin

Ivermectin 3 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1731

Product details

Brand name
Ivermectin
Generic name
Ivermectin
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216863
Marketed since
February 27, 2026
Listing expires
December 31, 2027
Pharmacologic class
Antiparasitic; Pediculicide

Active ingredients

Uses, dosage, side effects and warnings for Ivermectin →

Package NDC codes (1)

Package NDCDescriptionSince
70771-1731-32 BLISTER PACK in 1 CARTON (70771-1731-3) / 10 TABLET in 1 BLISTER PACK (70771-1731-2)Feb 27, 2026

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