Package 36000-033-10

Brand: metoprolol

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 36000-033-10
Digits Only 3600003310
Product NDC 36000-033
Description

10 VIAL in 1 CARTON (36000-033-10) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2012-09-25
Brand metoprolol
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5d975af3-d078-4130-9448-ed77123f1aac", "openfda": {"upc": ["0336000033107"], "unii": ["W5S57Y3A5L"], "rxcui": ["866508"], "spl_set_id": ["09566368-f91d-43a3-b683-30c844fb125a"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (36000-033-10)  / 5 mL in 1 VIAL", "package_ndc": "36000-033-10", "marketing_start_date": "20120925"}], "brand_name": "Metoprolol", "product_id": "36000-033_5d975af3-d078-4130-9448-ed77123f1aac", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "36000-033", "generic_name": "metoprolol tartrate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "5 mg/5mL"}], "application_number": "ANDA078950", "marketing_category": "ANDA", "marketing_start_date": "20120925", "listing_expiration_date": "20261231"}