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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-547
Product ID 72189-547_15d5c223-af4f-e803-e063-6294a90af3d8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203894
Listing Expiration 2026-12-31
Marketing Start 2024-04-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189547
Hyphenated Format 72189-547

Supplemental Identifiers

RxCUI
866436
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 ANDA203894 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-547-90)
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": "15d5c223-af4f-e803-e063-6294a90af3d8", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["15d5c223-af4e-e803-e063-6294a90af3d8"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-547-90)", "package_ndc": "72189-547-90", "marketing_start_date": "20240411"}], "brand_name": "Metoprolol Succinate ER", "product_id": "72189-547_15d5c223-af4f-e803-e063-6294a90af3d8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-547", "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": "50 mg/1"}], "application_number": "ANDA203894", "marketing_category": "ANDA", "marketing_start_date": "20240411", "listing_expiration_date": "20261231"}