# CROMOLYN SODIUM

NDC: 81665-104
Generic name: CROMOLYN SODIUM
Labeler / Manufacturer: Omnivium Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION, CONCENTRATE
Routes: ORAL
Marketing started: 20240831

FDA application: ANDA209264

## Active ingredients

- CROMOLYN SODIUM: 100 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81665-104"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81665-104
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a742664b-265e-49f9-9744-d04e1fb620ae