metoprolol succinate

Generic: metoprolol succinate

Labeler: oryza pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler oryza pharmaceuticals inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
Oryza pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 72516-026
Product ID 72516-026_3d4f2b14-3745-23c9-e063-6294a90aaa50
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214110
Listing Expiration 2026-12-31
Marketing Start 2025-07-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72516026
Hyphenated Format 72516-026

Supplemental Identifiers

RxCUI
866412 866419 866436
UPC
0372516026103 0372516028015 0372516027100
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 ANDA214110 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-026-10)
source: ndc

Packages (1)

Ingredients (1)

metoprolol succinate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d4f2b14-3745-23c9-e063-6294a90aaa50", "openfda": {"upc": ["0372516026103", "0372516028015", "0372516027100"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866436"], "spl_set_id": ["151079c5-6360-45ed-8118-885543d6a4ad"], "manufacturer_name": ["Oryza pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-026-10)", "package_ndc": "72516-026-10", "marketing_start_date": "20250721"}], "brand_name": "Metoprolol succinate", "product_id": "72516-026_3d4f2b14-3745-23c9-e063-6294a90aaa50", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72516-026", "generic_name": "Metoprolol succinate", "labeler_name": "Oryza pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA214110", "marketing_category": "ANDA", "marketing_start_date": "20250721", "listing_expiration_date": "20261231"}