FDA NDC Directory · JSON-LD · Markdown

Cromolyn Sodium Oral Solution (Concentrate)

NDC 76204-025 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE

Labeler / ManufacturerRitedose Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209264
Dosage form / routeSOLUTION, CONCENTRATE · ORAL
Active ingredientsCROMOLYN SODIUM (100 mg/5mL)
Marketing started20211201
Package count1

External sources

Source: openFDA. Public-domain (CC0).