NDC 70771-1109 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1109

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204331
Marketed since
August 9, 2017
Listing expires
December 31, 2026
Pharmacologic class
Dietary Cholesterol Absorption Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ezetimibe →

Package NDC codes (6)

Package NDCDescriptionSince
70771-1109-01000 TABLET in 1 BOTTLE (70771-1109-0)Aug 9, 2017
70771-1109-1100 TABLET in 1 BOTTLE (70771-1109-1)Aug 9, 2017
70771-1109-330 TABLET in 1 BOTTLE (70771-1109-3)Aug 9, 2017
70771-1109-410 BLISTER PACK in 1 CARTON (70771-1109-4) / 10 TABLET in 1 BLISTER PACK (70771-1109-2)Aug 9, 2017
70771-1109-5500 TABLET in 1 BOTTLE (70771-1109-5)Aug 9, 2017
70771-1109-990 TABLET in 1 BOTTLE (70771-1109-9)Aug 9, 2017

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