Package 68788-8490-1

Brand: cromolyn sodium

Generic: cromolyn sodium
NDC Package

Package Facts

Identity

Package NDC 68788-8490-1
Digits Only 6878884901
Product NDC 68788-8490
Product ID 68788-8490_aaddc929-8d3d-47fe-bb00-f2963df993c3
Description

10 mL in 1 BOTTLE, PLASTIC (68788-8490-1)

Marketing

Marketing Status
Marketed Since 2023-07-21
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": ["OPHTHALMIC"], "spl_id": "aaddc929-8d3d-47fe-bb00-f2963df993c3", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831109"], "spl_set_id": ["18892411-465f-4d8d-9550-7dafa6c6a0a3"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE, PLASTIC (68788-8490-1)", "package_ndc": "68788-8490-1", "marketing_start_date": "20230721"}], "brand_name": "Cromolyn Sodium", "product_id": "68788-8490_aaddc929-8d3d-47fe-bb00-f2963df993c3", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "68788-8490", "generic_name": "Cromolyn Sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cromolyn Sodium", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "40 mg/mL"}], "application_number": "ANDA075282", "marketing_category": "ANDA", "marketing_start_date": "20230721", "listing_expiration_date": "20261231"}