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Cromolyn Sodium

NDC 57782-397 · HUMAN OTC DRUG · SPRAY, METERED

Labeler / ManufacturerBausch & Lomb Incorporated
Marketing categoryAbbreviated NDA (generic) · App ANDA075702
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsCROMOLYN SODIUM (5.2 mg/1)
Marketing started20010703
Package count1

External sources

Source: openFDA. Public-domain (CC0).