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Omeprazole and Sodium Bicarbonate

NDC 27241-030 · HUMAN PRESCRIPTION DRUG · FOR SUSPENSION

Labeler / ManufacturerAjanta Pharma USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205545
Dosage form / routeFOR SUSPENSION · ORAL
Active ingredientsOMEPRAZOLE (40 mg/1)
SODIUM BICARBONATE (1680 mg/1)
Marketing started20160727
Package count2

External sources

Source: openFDA. Public-domain (CC0).