metoprolol succinate

Generic: metoprolol succinate

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler actavis pharma, inc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 45963-676
Product ID 45963-676_e51ef0b9-fe4a-473c-92a0-6043fdb0b620
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204161
Listing Expiration 2026-12-31
Marketing Start 2020-02-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 45963676
Hyphenated Format 45963-676

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 ANDA204161 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-11)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-96)
source: ndc

Packages (2)

45963-676-11 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-11) 45963-676-96 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-96)

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": "e51ef0b9-fe4a-473c-92a0-6043fdb0b620", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["b798601e-a369-4c8b-8235-08900e1b751d"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-11)", "package_ndc": "45963-676-11", "marketing_start_date": "20200203"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-676-96)", "package_ndc": "45963-676-96", "marketing_start_date": "20200203"}], "brand_name": "metoprolol succinate", "product_id": "45963-676_e51ef0b9-fe4a-473c-92a0-6043fdb0b620", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "45963-676", "generic_name": "metoprolol succinate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204161", "marketing_category": "ANDA", "marketing_start_date": "20200203", "listing_expiration_date": "20261231"}