metoprolol succinate

Generic: metoprolol succinate er tablets

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 er tablets
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5733
Product ID 50090-5733_96b4f61f-0809-491a-8047-218634477cf8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211143
Listing Expiration 2026-12-31
Marketing Start 2020-11-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905733
Hyphenated Format 50090-5733

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 (source: ndc)
Generic Name metoprolol succinate er tablets (source: ndc)
Application Number ANDA211143 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-0)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-1)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-3)
source: ndc

Packages (3)

50090-5733-0 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-0) 50090-5733-1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-1) 50090-5733-3 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-3)

Ingredients (1)

metoprolol succinate (25 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": "96b4f61f-0809-491a-8047-218634477cf8", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427"], "spl_set_id": ["b89de581-2a6f-4dc2-ae82-ae6a6a209966"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-0)", "package_ndc": "50090-5733-0", "marketing_start_date": "20210928"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-1)", "package_ndc": "50090-5733-1", "marketing_start_date": "20210928"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5733-3)", "package_ndc": "50090-5733-3", "marketing_start_date": "20210928"}], "brand_name": "Metoprolol Succinate", "product_id": "50090-5733_96b4f61f-0809-491a-8047-218634477cf8", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5733", "generic_name": "Metoprolol Succinate ER Tablets", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA211143", "marketing_category": "ANDA", "marketing_start_date": "20201127", "listing_expiration_date": "20261231"}