NDC 68382-773 – Ezetimibe

Ezetimibe 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-773

Product details

Brand name
Ezetimibe
Generic name
Ezetimibe
Labeler
Zydus Pharmaceuticals USA Inc.
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
68382-773-01100 TABLET in 1 BOTTLE (68382-773-01)Aug 9, 2017
68382-773-05500 TABLET in 1 BOTTLE (68382-773-05)Aug 9, 2017
68382-773-0630 TABLET in 1 BOTTLE (68382-773-06)Aug 9, 2017
68382-773-101000 TABLET in 1 BOTTLE (68382-773-10)Aug 9, 2017
68382-773-1690 TABLET in 1 BOTTLE (68382-773-16)Aug 9, 2017
68382-773-7710 BLISTER PACK in 1 CARTON (68382-773-77) / 10 TABLET in 1 BLISTER PACK (68382-773-30)Aug 9, 2017

Other Ezetimibe products