metoprolol tartrate

Generic: metoprolol tartrate

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler coupler llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoprolol tartrate 25 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1561
Product ID 67046-1561_36988969-ac67-58c9-e063-6294a90a01f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2026-12-31
Marketing Start 2025-06-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 670461561
Hyphenated Format 67046-1561

Supplemental Identifiers

RxCUI
866924
UPC
0372888208008
UNII
W5S57Y3A5L

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (67046-1561-3)
source: ndc

Packages (1)

Ingredients (1)

metoprolol tartrate (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36988969-ac67-58c9-e063-6294a90a01f5", "openfda": {"upc": ["0372888208008"], "unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["3698837b-c34b-569a-e063-6394a90a167c"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1561-3)", "package_ndc": "67046-1561-3", "marketing_start_date": "20250602"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "67046-1561_36988969-ac67-58c9-e063-6294a90a01f5", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67046-1561", "generic_name": "METOPROLOL TARTRATE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20250602", "listing_expiration_date": "20261231"}