metoprolol succinate

Generic: metoprolol succinate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7239
Product ID 50090-7239_92658b35-7389-4451-a769-18ebb18e081c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090617
Listing Expiration 2026-12-31
Marketing Start 2023-04-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907239
Hyphenated Format 50090-7239

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 (source: ndc)
Generic Name metoprolol succinate (source: ndc)
Application Number ANDA090617 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7239-0)
source: ndc

Packages (1)

50090-7239-0 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7239-0)

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": "92658b35-7389-4451-a769-18ebb18e081c", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["46c288aa-a55c-4207-9a6e-ceef3c2f60ff"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7239-0)", "package_ndc": "50090-7239-0", "marketing_start_date": "20240910"}], "brand_name": "Metoprolol succinate", "product_id": "50090-7239_92658b35-7389-4451-a769-18ebb18e081c", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7239", "generic_name": "Metoprolol succinate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA090617", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}