metoprolol succinate

Generic: metoprolol succinate

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler northstar rx llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 50 mg/1

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 72603-143
Product ID 72603-143_82de0ba4-1cc6-e9d1-7dc3-844ff6ec1fb3
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 72603143
Hyphenated Format 72603-143

Supplemental Identifiers

RxCUI
866427 866436
UPC
0372603143010 0372603142013
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 ANDA090617 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-02)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-03)
source: ndc

Packages (3)

72603-143-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-01) 72603-143-02 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-02) 72603-143-03 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-03)

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": "82de0ba4-1cc6-e9d1-7dc3-844ff6ec1fb3", "openfda": {"upc": ["0372603143010", "0372603142013"], "unii": ["TH25PD4CCB"], "rxcui": ["866427", "866436"], "spl_set_id": ["ad097646-cc77-8d67-5974-cc00060409f2"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-01)", "package_ndc": "72603-143-01", "marketing_start_date": "20230410"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-02)", "package_ndc": "72603-143-02", "marketing_start_date": "20230410"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-03)", "package_ndc": "72603-143-03", "marketing_start_date": "20230912"}], "brand_name": "Metoprolol succinate", "product_id": "72603-143_82de0ba4-1cc6-e9d1-7dc3-844ff6ec1fb3", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72603-143", "generic_name": "Metoprolol succinate", "labeler_name": "Northstar Rx LLC", "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"}