NDC 67877-445 – Olmesartan Medoxomil

Olmesartan Medoxomil 5 mg/1 · Tablet, Coated · Oral

Human Prescription Drug 2 recalls

Product NDC67877-445

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA206763
Marketed since
April 24, 2017
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Olmesartan Medoxomil →

Package NDC codes (4)

Package NDCDescriptionSince
67877-445-05500 TABLET, COATED in 1 BOTTLE (67877-445-05)Apr 24, 2017
67877-445-101000 TABLET, COATED in 1 BOTTLE (67877-445-10)Apr 24, 2017
67877-445-3030 TABLET, COATED in 1 BOTTLE (67877-445-30)Apr 24, 2017
67877-445-9090 TABLET, COATED in 1 BOTTLE (67877-445-90)Apr 24, 2017

Recalls mentioning this NDC

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