Package 57782-397-26

Brand: cromolyn sodium

Generic: cromolyn sodium
NDC Package

Package Facts

Identity

Package NDC 57782-397-26
Digits Only 5778239726
Product NDC 57782-397
Description

1 BOTTLE in 1 CARTON (57782-397-26) / 200 SPRAY, METERED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2001-07-03
Brand cromolyn sodium
Generic cromolyn sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "d66445c2-3e1d-458a-9c62-d4fc2ef4ec8f", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["1797851"], "spl_set_id": ["379f4b59-6866-4b5c-9b1b-d8a35b741461"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (57782-397-26)  / 200 SPRAY, METERED in 1 BOTTLE", "package_ndc": "57782-397-26", "marketing_start_date": "20010703"}], "brand_name": "Cromolyn Sodium", "product_id": "57782-397_d66445c2-3e1d-458a-9c62-d4fc2ef4ec8f", "dosage_form": "SPRAY, METERED", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "57782-397", "generic_name": "Cromolyn Sodium", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cromolyn Sodium", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "5.2 mg/1"}], "application_number": "ANDA075702", "marketing_category": "ANDA", "marketing_start_date": "20010703", "listing_expiration_date": "20261231"}