Package 43063-762-30

Brand: montelukast sodium

Generic: montelukast sodium
NDC Package

Package Facts

Identity

Package NDC 43063-762-30
Digits Only 4306376230
Product NDC 43063-762
Product ID 43063-762_414b7ce2-7550-5e40-e063-6294a90afda2
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-762-30)

Marketing

Marketing Status
Marketed Since 2017-05-04
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": "414b7ce2-7550-5e40-e063-6294a90afda2", "openfda": {"upc": ["0343063762301"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["c9ec1996-6a54-4622-b8a6-57dea49f6b35"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-762-30)", "package_ndc": "43063-762-30", "marketing_start_date": "20170504"}], "brand_name": "Montelukast Sodium", "product_id": "43063-762_414b7ce2-7550-5e40-e063-6294a90afda2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "43063-762", "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": "ANDA202717", "marketing_category": "ANDA", "marketing_start_date": "20130411", "listing_expiration_date": "20261231"}