Discontinued
Strength
40; 1680 mg/1; mg/1
Manufacturer
Oceanside PharmaceuticalsNDC
68682099130
Classification
Generic
Dosage Form
POWDER, FOR SUSPENSION
Route
ORAL
Last Updated
9/17/2025
Active Ingredients
OMEPRAZOLE; SODIUM BICARBONATEApproval Type
Authorized Generic (NDA)
FDA Application
NDA021636On Market Since
6/15/2004
Pharmacological Classes
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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