metoprolol tartrate
Generic: metoprolol tartrate
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
metoprolol tartrate
Generic Name
metoprolol tartrate
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
metoprolol tartrate 1 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04091778
Hyphenated Format
0409-1778
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1778-05) / 5 mL in 1 VIAL, SINGLE-DOSE (0409-1778-15)
Packages (1)
Ingredients (1)
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"}