metoprolol succinate

Generic: metoprolol succinate

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler northwind health company, llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 100 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-079
Product ID 82868-079_4720215f-ae95-5f51-e063-6394a90ab4c2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216916
Listing Expiration 2026-12-31
Marketing Start 2025-06-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82868079
Hyphenated Format 82868-079

Supplemental Identifiers

RxCUI
866412
UNII
TH25PD4CCB

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 succinate (source: ndc)
Generic Name metoprolol succinate (source: ndc)
Application Number ANDA216916 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-30)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-90)
source: ndc

Packages (2)

82868-079-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-30) 82868-079-90 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-90)

Ingredients (1)

metoprolol succinate (100 mg/1)

Linked Drug Pages (1)

Metoprolol Succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4720215f-ae95-5f51-e063-6394a90ab4c2", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412"], "spl_set_id": ["47202157-3f32-275d-e063-6294a90a5c44"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-30)", "package_ndc": "82868-079-30", "marketing_start_date": "20250930"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-90)", "package_ndc": "82868-079-90", "marketing_start_date": "20250606"}], "brand_name": "Metoprolol Succinate", "product_id": "82868-079_4720215f-ae95-5f51-e063-6394a90ab4c2", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82868-079", "generic_name": "Metoprolol Succinate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA216916", "marketing_category": "ANDA", "marketing_start_date": "20250606", "listing_expiration_date": "20261231"}