metoprolol succinate
Generic: metoprolol succinate
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
metoprolol succinate
Generic Name
metoprolol succinate
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
metoprolol succinate 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
45963-678
Product ID
45963-678_e51ef0b9-fe4a-473c-92a0-6043fdb0b620
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204161
Listing Expiration
2026-12-31
Marketing Start
2019-10-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
45963678
Hyphenated Format
45963-678
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-678-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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 (45963-678-11)", "package_ndc": "45963-678-11", "marketing_start_date": "20191023"}], "brand_name": "metoprolol succinate", "product_id": "45963-678_e51ef0b9-fe4a-473c-92a0-6043fdb0b620", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "45963-678", "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": "200 mg/1"}], "application_number": "ANDA204161", "marketing_category": "ANDA", "marketing_start_date": "20191023", "listing_expiration_date": "20261231"}