metoprolol succinate

Generic: metoprolol succinate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler proficient rx lp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-014
Product ID 82804-014_502653e6-1971-4abf-9b21-ba0a9957672b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207206
Listing Expiration 2026-12-31
Marketing Start 2022-04-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804014
Hyphenated Format 82804-014

Supplemental Identifiers

RxCUI
866436
UPC
0382804014903
UNII
W5S57Y3A5L

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 ANDA207206 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-90)
source: ndc

Packages (3)

Ingredients (1)

metoprolol tartrate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "502653e6-1971-4abf-9b21-ba0a9957672b", "openfda": {"upc": ["0382804014903"], "unii": ["W5S57Y3A5L"], "rxcui": ["866436"], "spl_set_id": ["502653e6-1971-4abf-9b21-ba0a9957672b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-30)", "package_ndc": "82804-014-30", "marketing_start_date": "20231003"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-60)", "package_ndc": "82804-014-60", "marketing_start_date": "20231003"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-90)", "package_ndc": "82804-014-90", "marketing_start_date": "20231003"}], "brand_name": "Metoprolol Succinate", "product_id": "82804-014_502653e6-1971-4abf-9b21-ba0a9957672b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82804-014", "generic_name": "Metoprolol Succinate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA207206", "marketing_category": "ANDA", "marketing_start_date": "20220427", "listing_expiration_date": "20261231"}