Package 0378-0032-01

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 0378-0032-01
Digits Only 0378003201
Product NDC 0378-0032
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0032-01)

Marketing

Marketing Status
Marketed Since 1993-12-23
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "57d60035-d408-4f98-932e-2cbbeae5326c", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924", "1606347", "1606349"], "spl_set_id": ["809c6386-0039-42ff-a03e-e42733e229b8"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0032-01)", "package_ndc": "0378-0032-01", "marketing_start_date": "19931223"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0032-10)", "package_ndc": "0378-0032-10", "marketing_start_date": "19931223"}], "brand_name": "Metoprolol Tartrate", "product_id": "0378-0032_57d60035-d408-4f98-932e-2cbbeae5326c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0378-0032", "generic_name": "metoprolol tartrate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA076704", "marketing_category": "ANDA", "marketing_start_date": "19931223", "listing_expiration_date": "20261231"}