metoprolol succinate

Generic: metoprolol succinate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 25 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-4022
Product ID 68788-4022_27bb8bd5-b3ae-4eb3-b508-5684904408be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216916
Listing Expiration 2026-12-31
Marketing Start 2025-09-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687884022
Hyphenated Format 68788-4022

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 (source: ndc)
Application Number ANDA216916 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-3)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-6)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-9)
source: ndc

Packages (3)

68788-4022-3 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-3) 68788-4022-6 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-6) 68788-4022-9 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-9)

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": "27bb8bd5-b3ae-4eb3-b508-5684904408be", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427"], "spl_set_id": ["27bb8bd5-b3ae-4eb3-b508-5684904408be"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-3)", "package_ndc": "68788-4022-3", "marketing_start_date": "20250905"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-6)", "package_ndc": "68788-4022-6", "marketing_start_date": "20250905"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-9)", "package_ndc": "68788-4022-9", "marketing_start_date": "20250905"}], "brand_name": "Metoprolol Succinate", "product_id": "68788-4022_27bb8bd5-b3ae-4eb3-b508-5684904408be", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-4022", "generic_name": "Metoprolol Succinate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA216916", "marketing_category": "ANDA", "marketing_start_date": "20250905", "listing_expiration_date": "20261231"}