metoprolol succinate er

Generic: metoprolol succinate er

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate er
Generic Name metoprolol succinate er
Labeler direct_rx
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 25 mg/1

Manufacturer
DIrect_Rx

Identifiers & Regulatory

Product NDC 72189-652
Product ID 72189-652_45723206-1a9e-5299-e063-6294a90ad969
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216916
Listing Expiration 2026-12-31
Marketing Start 2025-12-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189652
Hyphenated Format 72189-652

Supplemental Identifiers

RxCUI
866427
UNII
TH25PD4CCB

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 er (source: ndc)
Generic Name metoprolol succinate er (source: ndc)
Application Number ANDA216916 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-652-90)
source: ndc

Packages (1)

Ingredients (1)

metoprolol succinate (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45723206-1a9e-5299-e063-6294a90ad969", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427"], "spl_set_id": ["45723206-1a9d-5299-e063-6294a90ad969"], "manufacturer_name": ["DIrect_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-652-90)", "package_ndc": "72189-652-90", "marketing_start_date": "20251208"}], "brand_name": "Metoprolol Succinate ER", "product_id": "72189-652_45723206-1a9e-5299-e063-6294a90ad969", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-652", "generic_name": "Metoprolol Succinate ER", "labeler_name": "DIrect_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate ER", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA216916", "marketing_category": "ANDA", "marketing_start_date": "20251208", "listing_expiration_date": "20261231"}