Package 68071-5236-1

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package Sample

Package Facts

Identity

Package NDC 68071-5236-1
Digits Only 6807152361
Product NDC 68071-5236
Description

100 TABLET, FILM COATED in 1 BOTTLE (68071-5236-1)

Marketing

Marketing Status
Marketed Since 2020-04-03
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b5932a3-78ed-5fbb-e063-6394a90a8174", "openfda": {"upc": ["0368071523614"], "unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["a2669da1-b712-5fd5-e053-2a95a90a52f3"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68071-5236-1)", "package_ndc": "68071-5236-1", "marketing_start_date": "20200403"}], "brand_name": "Metoprolol Tartrate", "product_id": "68071-5236_1b5932a3-78ed-5fbb-e063-6394a90a8174", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-5236", "generic_name": "Metoprolol Tartrate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}