metoprolol tartrate
Generic: metoprolol tartrate
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
metoprolol tartrate
Generic Name
metoprolol tartrate
Labeler
american health packaging
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
metoprolol tartrate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62584-266
Product ID
62584-266_2e966478-1706-ae7a-e063-6394a90a9a8e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077739
Listing Expiration
2026-12-31
Marketing Start
2010-06-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62584266
Hyphenated Format
62584-266
Supplemental Identifiers
RxCUI
UNII
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
ANDA077739 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (62584-266-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (62584-266-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e966478-1706-ae7a-e063-6394a90a9a8e", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924"], "spl_set_id": ["0a3ccfd4-8b65-4c7e-b0ba-27ff40d5b5e8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (62584-266-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (62584-266-11)", "package_ndc": "62584-266-01", "marketing_start_date": "20100622"}], "brand_name": "Metoprolol Tartrate", "product_id": "62584-266_2e966478-1706-ae7a-e063-6394a90a9a8e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62584-266", "generic_name": "Metoprolol Tartrate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20100622", "listing_expiration_date": "20261231"}