Package 42571-350-09

Brand: cromolyn sodium

Generic: cromolyn sodium
NDC Package

Package Facts

Identity

Package NDC 42571-350-09
Digits Only 4257135009
Product NDC 42571-350
Product ID 42571-350_22feddbf-0d9b-8ce7-e063-6394a90a8887
Description

5 CARTON in 1 CARTON (42571-350-09) / 12 AMPULE in 1 CARTON / 2 mL in 1 AMPULE (42571-350-08)

Marketing

Marketing Status
Marketed Since 2022-06-01
Brand cromolyn sodium
Generic cromolyn sodium
Sample Package No

Linked Drug Pages (1)

Cromolyn Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRABRONCHIAL"], "spl_id": "22feddbf-0d9b-8ce7-e063-6394a90a8887", "openfda": {"upc": ["0342571350086"], "unii": ["Q2WXR1I0PK"], "rxcui": ["831246"], "spl_set_id": ["aebec664-ed80-447c-9789-0cf47c8b7429"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 CARTON in 1 CARTON (42571-350-09)  / 12 AMPULE in 1 CARTON / 2 mL in 1 AMPULE (42571-350-08)", "package_ndc": "42571-350-09", "marketing_start_date": "20220601"}, {"sample": false, "description": "10 CARTON in 1 CARTON (42571-350-50)  / 12 AMPULE in 1 CARTON / 2 mL in 1 AMPULE (42571-350-08)", "package_ndc": "42571-350-50", "marketing_start_date": "20220601"}], "brand_name": "Cromolyn Sodium", "product_id": "42571-350_22feddbf-0d9b-8ce7-e063-6394a90a8887", "dosage_form": "INHALANT", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "42571-350", "generic_name": "Cromolyn Sodium", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cromolyn Sodium", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "20 mg/2mL"}], "application_number": "ANDA213658", "marketing_category": "ANDA", "marketing_start_date": "20220601", "listing_expiration_date": "20261231"}