FDA NDC Directory · JSON-LD · Markdown

CROMOLYN SODIUM

NDC 42571-132 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE

Generic nameCromolyn sodium
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202745
Dosage form / routeSOLUTION, CONCENTRATE · ORAL
Active ingredientsCROMOLYN SODIUM (100 mg/5mL)
Marketing started20130504
Package count1

External sources

Source: openFDA. Public-domain (CC0).