# Cromolyn Sodium

NDC: 57782-397
Generic name: Cromolyn Sodium
Labeler / Manufacturer: Bausch & Lomb Incorporated
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY, METERED
Routes: NASAL
Marketing started: 20010703

FDA application: ANDA075702

## Active ingredients

- CROMOLYN SODIUM: 5.2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57782-397"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57782-397
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=379f4b59-6866-4b5c-9b1b-d8a35b741461