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Omeprazole and Sodium Bicarbonate

NDC 43598-307 · HUMAN OTC DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerDr. Reddy's Laboratories Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA217784
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
SODIUM BICARBONATE (1680 mg/1)
Marketing started20240715
Package count4

External sources

Source: openFDA. Public-domain (CC0).