metoprolol succinate
Generic: metoprolol succinate er tablets
Labeler: ascend laboratories, llcDrug 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
Active Ingredients
metoprolol succinate 200 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67877593
Hyphenated Format
67877-593
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 200 mg/1
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)
Packages (5)
67877-593-01
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-01)
67877-593-05
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-05)
67877-593-10
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-10)
67877-593-30
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-30)
67877-593-60
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-60)
Ingredients (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"}