metoprolol succinate

Generic: metoprolol succinate er tablets

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate er tablets
Labeler ascend laboratories, llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 200 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-593
Product ID 67877-593_7b6e362b-e8bc-45ee-b369-7109fb60adeb
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 67877593
Hyphenated Format 67877-593

Supplemental Identifiers

RxCUI
866412 866419 866427 866436
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 er tablets (source: ndc)
Application Number ANDA211143 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-05)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-10)
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-30)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-60)
source: ndc

Packages (5)

Ingredients (1)

metoprolol succinate (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7b6e362b-e8bc-45ee-b369-7109fb60adeb", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866419", "866427", "866436"], "spl_set_id": ["58441cd3-6043-4bb8-adab-1b32a203bfb2"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-01)", "package_ndc": "67877-593-01", "marketing_start_date": "20201127"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-05)", "package_ndc": "67877-593-05", "marketing_start_date": "20250220"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-10)", "package_ndc": "67877-593-10", "marketing_start_date": "20201127"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-30)", "package_ndc": "67877-593-30", "marketing_start_date": "20201127"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-60)", "package_ndc": "67877-593-60", "marketing_start_date": "20201127"}], "brand_name": "Metoprolol Succinate", "product_id": "67877-593_7b6e362b-e8bc-45ee-b369-7109fb60adeb", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67877-593", "generic_name": "Metoprolol Succinate ER Tablets", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "200 mg/1"}], "application_number": "ANDA211143", "marketing_category": "ANDA", "marketing_start_date": "20201127", "listing_expiration_date": "20261231"}