metoprolol succinate

Generic: metoprolol succinate

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler epic pharma, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-725
Product ID 42806-725_2c74614f-0615-6839-e063-6294a90acc19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213854
Listing Expiration 2026-12-31
Marketing Start 2025-02-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806725
Hyphenated Format 42806-725

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
UNII
TH25PD4CCB

Packaging Origin

Original Packager
true

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 ANDA213854 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-05)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-10)
source: ndc

Packages (3)

42806-725-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-01) 42806-725-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-05) 42806-725-10 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-10)

Ingredients (1)

metoprolol succinate (50 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": "2c74614f-0615-6839-e063-6294a90acc19", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["2c70177a-615b-4ed7-a58f-a298212e8fae"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-01)", "package_ndc": "42806-725-01", "marketing_start_date": "20250201"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-05)", "package_ndc": "42806-725-05", "marketing_start_date": "20250201"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-725-10)", "package_ndc": "42806-725-10", "marketing_start_date": "20250201"}], "brand_name": "Metoprolol succinate", "product_id": "42806-725_2c74614f-0615-6839-e063-6294a90acc19", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42806-725", "generic_name": "Metoprolol succinate", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA213854", "marketing_category": "ANDA", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}