NDC 68682-102 – Omeprazole and Sodium Bicarbonate

Omeprazole 20 mg/1; Sodium Bicarbonate 1100 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC68682-102

Product details

Brand name
Omeprazole and Sodium Bicarbonate
Generic name
omeprazole, sodium bicarbonate
Labeler
Oceanside Pharmaceuticals
Dosage form
Capsule
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021849
Marketed since
February 27, 2006
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole and Sodium Bicarbonate →

Package NDC codes (1)

Package NDCDescriptionSince
68682-102-3030 CAPSULE in 1 BOTTLE (68682-102-30)Feb 27, 2006

Recalls mentioning this NDC

Other Omeprazole and Sodium Bicarbonate products