Package 81665-104-96

Brand: cromolyn sodium

Generic: cromolyn sodium
NDC Package

Package Facts

Identity

Package NDC 81665-104-96
Digits Only 8166510496
Product NDC 81665-104
Product ID 81665-104_fd09b0f1-907c-4d4d-a693-9756efd60f20
Description

12 POUCH in 1 CARTON (81665-104-96) / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2024-08-31
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": ["ORAL"], "spl_id": "fd09b0f1-907c-4d4d-a693-9756efd60f20", "openfda": {"unii": ["Q2WXR1I0PK"], "rxcui": ["831261"], "spl_set_id": ["a742664b-265e-49f9-9744-d04e1fb620ae"], "manufacturer_name": ["Omnivium Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CARTON (81665-104-96)  / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE", "package_ndc": "81665-104-96", "marketing_start_date": "20240831"}], "brand_name": "CROMOLYN SODIUM", "product_id": "81665-104_fd09b0f1-907c-4d4d-a693-9756efd60f20", "dosage_form": "SOLUTION, CONCENTRATE", "pharm_class": ["Decreased Histamine Release [PE]", "Mast Cell Stabilizer [EPC]"], "product_ndc": "81665-104", "generic_name": "CROMOLYN SODIUM", "labeler_name": "Omnivium Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CROMOLYN SODIUM", "active_ingredients": [{"name": "CROMOLYN SODIUM", "strength": "100 mg/5mL"}], "application_number": "ANDA209264", "marketing_category": "ANDA", "marketing_start_date": "20240831", "listing_expiration_date": "20271231"}