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 tartrate 100 mg/1

Manufacturer
Oryza Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 72516-032
Product ID 72516-032_2b4bd7b3-d6df-e98e-e063-6394a90a7f9d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207206
Listing Expiration 2026-12-31
Marketing Start 2022-04-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72516032
Hyphenated Format 72516-032

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
UPC
0372516030018 0372516033019 0372516031015
UNII
W5S57Y3A5L

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 ANDA207206 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-032-01)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-032-10)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-032-50)
source: ndc

Packages (3)

Ingredients (1)

metoprolol tartrate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b4bd7b3-d6df-e98e-e063-6394a90a7f9d", "openfda": {"upc": ["0372516030018", "0372516033019", "0372516031015"], "unii": ["W5S57Y3A5L"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["6cfe96df-bd75-432d-b2c2-e26143ca36dd"], "manufacturer_name": ["Oryza Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-032-01)", "package_ndc": "72516-032-01", "marketing_start_date": "20220427"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-032-10)", "package_ndc": "72516-032-10", "marketing_start_date": "20220427"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-032-50)", "package_ndc": "72516-032-50", "marketing_start_date": "20220427"}], "brand_name": "Metoprolol Succinate", "product_id": "72516-032_2b4bd7b3-d6df-e98e-e063-6394a90a7f9d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72516-032", "generic_name": "Metoprolol Succinate", "labeler_name": "Oryza Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA207206", "marketing_category": "ANDA", "marketing_start_date": "20220427", "listing_expiration_date": "20261231"}