Package 72789-306-30

Brand: montelukast sodium

Generic: montelukast sodium
NDC Package

Package Facts

Identity

Package NDC 72789-306-30
Digits Only 7278930630
Product NDC 72789-306
Product ID 72789-306_40bb0181-d383-4540-e063-6394a90a8e46
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-306-30)

Marketing

Marketing Status
Marketed Since 2022-03-06
Brand montelukast sodium
Generic montelukast sodium
Sample Package No

Linked Drug Pages (1)

Montelukast Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40bb0181-d383-4540-e063-6394a90a8e46", "openfda": {"upc": ["0372789306308"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["6ffff72c-8784-477b-8722-5434a19881a0"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-306-30)", "package_ndc": "72789-306-30", "marketing_start_date": "20220306"}], "brand_name": "Montelukast Sodium", "product_id": "72789-306_40bb0181-d383-4540-e063-6394a90a8e46", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "72789-306", "generic_name": "Montelukast Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast Sodium", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA202468", "marketing_category": "ANDA", "marketing_start_date": "20120803", "listing_expiration_date": "20261231"}