Composition
- Active ingredients
- OMEPRAZOLE 40MG/PACKET; SODIUM BICARBONATE 1.68GM/PACKET
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- OMEPRAZOLE 40MG; SODIUM BICARBONATE 1.1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · CapsuleNDA021849-002 · Discontinued
- OMEPRAZOLE 20MG; SODIUM BICARBONATE 1.1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · CapsuleNDA021849-001 · Discontinued
- OMEPRAZOLE 40MG/PACKET; SODIUM BICARBONATE 1.68GM/PACKET · For suspensionThis page
- OMEPRAZOLE 20MG/PACKET; SODIUM BICARBONATE 1.68GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · For suspensionNDA021636-001 · Discontinued
- OMEPRAZOLE 40MG/PACKET; SODIUM BICARBONATE 1.68GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · For suspensionNDA021636-002 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA021706.
At a glance
- Brand name
- Zegerid
- Active substance
- omeprazole
- Route
- Oral
- Dosage form
- For suspension
- Applicant
- Santarus
- Status
- Discontinued
- FDA approval
- 21 Dec 2004
- Application
- NDA021706-001