metoprolol tartrate
Generic: metoprolol tartrate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
metoprolol tartrate
Generic Name
metoprolol tartrate
Labeler
proficient rx lp
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
metoprolol tartrate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-165
Product ID
82804-165_3c43fe89-2283-482e-9d97-648d3ed183f8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200981
Listing Expiration
2026-12-31
Marketing Start
2018-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804165
Hyphenated Format
82804-165
Supplemental Identifiers
RxCUI
UPC
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
ANDA200981 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (82804-165-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c43fe89-2283-482e-9d97-648d3ed183f8", "openfda": {"upc": ["0382804165902"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["3c43fe89-2283-482e-9d97-648d3ed183f8"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-165-90)", "package_ndc": "82804-165-90", "marketing_start_date": "20241216"}], "brand_name": "Metoprolol Tartrate", "product_id": "82804-165_3c43fe89-2283-482e-9d97-648d3ed183f8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82804-165", "generic_name": "Metoprolol Tartrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}