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Dextromethorphan Hydrobromide and Quinidine Sulphate

NDC 63304-650 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204196
Dosage form / routeCAPSULE · ORAL
Active ingredientsDEXTROMETHORPHAN HYDROBROMIDE (20 mg/1)
QUINIDINE SULFATE (10 mg/1)
Marketing started20260730
Package count1

External sources

Source: openFDA. Public-domain (CC0).