metoprolol succinate
Generic: metoprolol succinate er tablets
Labeler: a-s medication solutionsDrug 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
Active Ingredients
metoprolol succinate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5723
Product ID
50090-5723_6bcb7236-a6fe-449b-a3bb-8c7dbe77e2b8
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
500905723
Hyphenated Format
50090-5723
Supplemental Identifiers
RxCUI
UNII
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
- 50 mg/1
Packaging
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5723-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6bcb7236-a6fe-449b-a3bb-8c7dbe77e2b8", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["c8c02764-ef49-4ee4-a3b1-9660cf0e582d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5723-0)", "package_ndc": "50090-5723-0", "marketing_start_date": "20210927"}], "brand_name": "Metoprolol Succinate", "product_id": "50090-5723_6bcb7236-a6fe-449b-a3bb-8c7dbe77e2b8", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5723", "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": "50 mg/1"}], "application_number": "ANDA211143", "marketing_category": "ANDA", "marketing_start_date": "20201127", "listing_expiration_date": "20261231"}