FDA NDC Directory · JSON-LD · Markdown

CROMOLYN SODIUM

NDC 81665-104 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE

Labeler / ManufacturerOmnivium Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209264
Dosage form / routeSOLUTION, CONCENTRATE · ORAL
Active ingredientsCROMOLYN SODIUM (100 mg/5mL)
Marketing started20240831
Package count1

External sources

Source: openFDA. Public-domain (CC0).