Package 43063-841-30

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 43063-841-30
Digits Only 4306384130
Product NDC 43063-841
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-841-30)

Marketing

Marketing Status
Marketed Since 2018-03-07
Brand metoprolol succinate
Generic metoprolol succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ed99919-d85e-beec-e063-6394a90a1083", "openfda": {"upc": ["0343063841303"], "unii": ["TH25PD4CCB"], "rxcui": ["866412"], "spl_set_id": ["189b6a89-8de8-4a62-a54b-a6c52be870ca"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-841-30)", "package_ndc": "43063-841-30", "marketing_start_date": "20180307"}], "brand_name": "Metoprolol succinate", "product_id": "43063-841_3ed99919-d85e-beec-e063-6394a90a1083", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43063-841", "generic_name": "Metoprolol succinate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078889", "marketing_category": "ANDA", "marketing_start_date": "20120910", "listing_expiration_date": "20261231"}