metoprolol tartrate

Generic: metoprolol tartrate

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

metoprolol tartrate 1 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-1778
Product ID 0409-1778_3f4f1186-294b-4192-b024-83f7615f8bf3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078085
Listing Expiration 2026-12-31
Marketing Start 2008-07-24

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04091778
Hyphenated Format 0409-1778

Supplemental Identifiers

RxCUI
866508
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 tartrate (source: ndc)
Generic Name metoprolol tartrate (source: ndc)
Application Number ANDA078085 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1778-05) / 5 mL in 1 VIAL, SINGLE-DOSE (0409-1778-15)
source: ndc

Packages (1)

Ingredients (1)

metoprolol tartrate (1 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3f4f1186-294b-4192-b024-83f7615f8bf3", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866508"], "spl_set_id": ["7c1f998a-233d-4feb-6ea2-457702abd0d2"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1778-05)  / 5 mL in 1 VIAL, SINGLE-DOSE (0409-1778-15)", "package_ndc": "0409-1778-05", "marketing_start_date": "20080724"}], "brand_name": "Metoprolol Tartrate", "product_id": "0409-1778_3f4f1186-294b-4192-b024-83f7615f8bf3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0409-1778", "generic_name": "METOPROLOL TARTRATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA078085", "marketing_category": "ANDA", "marketing_start_date": "20080724", "listing_expiration_date": "20261231"}