metoprolol

Generic: metoprolol tartrate

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol
Generic Name metoprolol tartrate
Labeler baxter healthcare corporation
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

metoprolol tartrate 5 mg/5mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 36000-033
Product ID 36000-033_5d975af3-d078-4130-9448-ed77123f1aac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078950
Listing Expiration 2026-12-31
Marketing Start 2012-09-25

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 36000033
Hyphenated Format 36000-033

Supplemental Identifiers

RxCUI
866508
UPC
0336000033107
UNII
W5S57Y3A5L

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name metoprolol (source: ndc)
Generic Name metoprolol tartrate (source: ndc)
Application Number ANDA078950 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (36000-033-10) / 5 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

metoprolol tartrate (5 mg/5mL)

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"}