metoprolol succinate (50742-616)

Drug Facts

Product Profile

Brand Name metoprolol succinate

Generic Name metoprolol succinate

Labeler ingenus pharmaceuticals, llc

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer

Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-616

Product ID 50742-616_3d94f6c6-d712-41ec-99e2-bf119e92f469

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA204106

Listing Expiration 2026-12-31

Marketing Start 2018-02-06

Pharmacologic Class

Classes

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742616

Hyphenated Format 50742-616

Supplemental Identifiers

RxCUI

866412 866419 866427 866436

UPC

0350742615018 0350742616015

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 ANDA204106 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

50 mg/1

source: ndc

Packaging

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-01)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-05)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-10)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-90)
57692 TABLET, EXTENDED RELEASE in 1 DRUM (50742-616-99)

source: ndc

Packages (5)

50742-616-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-01) 50742-616-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-05) 50742-616-10 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-10) 50742-616-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-90) 50742-616-99 57692 TABLET, EXTENDED RELEASE in 1 DRUM (50742-616-99)

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": "3d94f6c6-d712-41ec-99e2-bf119e92f469", "openfda": {"upc": ["0350742615018", "0350742616015"], "unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["9dcd1fdf-a651-48d4-8033-e5749d5f5650"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-01)", "package_ndc": "50742-616-01", "marketing_start_date": "20180206"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-05)", "package_ndc": "50742-616-05", "marketing_start_date": "20180206"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-10)", "package_ndc": "50742-616-10", "marketing_start_date": "20180206"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-616-90)", "package_ndc": "50742-616-90", "marketing_start_date": "20180206"}, {"sample": false, "description": "57692 TABLET, EXTENDED RELEASE in 1 DRUM (50742-616-99)", "package_ndc": "50742-616-99", "marketing_start_date": "20210409"}], "brand_name": "Metoprolol Succinate", "product_id": "50742-616_3d94f6c6-d712-41ec-99e2-bf119e92f469", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50742-616", "generic_name": "Metoprolol succinate", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204106", "marketing_category": "ANDA", "marketing_start_date": "20180206", "listing_expiration_date": "20261231"}