FDA NDC Directory · JSON-LD · Markdown

Citalopram Hydrobromide

NDC 65862-074 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077812
Dosage form / routeSOLUTION · ORAL
Active ingredientsCITALOPRAM HYDROBROMIDE (10 mg/5mL)
Marketing started20060828
Package count1

External sources

Source: openFDA. Public-domain (CC0).