# CROMOLYN SODIUM

NDC: 42571-132
Generic name: Cromolyn sodium
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION, CONCENTRATE
Routes: ORAL
Marketing started: 20130504

FDA application: ANDA202745

## Active ingredients

- CROMOLYN SODIUM: 100 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-132"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-132
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=93f80edb-3b38-423e-8cd6-5b5cb4393ec2