metoprolol succinate

Generic: metoprolol succinate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC 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 succinate 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-162
Product ID 71205-162_cc58a663-d683-41fb-bf47-1e07ffaa0fe0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA019962
Listing Expiration 2026-12-31
Marketing Start 2018-01-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205162
Hyphenated Format 71205-162

Supplemental Identifiers

RxCUI
866436
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 NDA019962 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-90)
source: ndc

Packages (3)

71205-162-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-30) 71205-162-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-60) 71205-162-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-90)

Ingredients (1)

metoprolol succinate (50 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": "cc58a663-d683-41fb-bf47-1e07ffaa0fe0", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["e236f1ed-b400-4854-81c7-64964422a2f7"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-30)", "package_ndc": "71205-162-30", "marketing_start_date": "20181101"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-60)", "package_ndc": "71205-162-60", "marketing_start_date": "20181101"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-90)", "package_ndc": "71205-162-90", "marketing_start_date": "20181101"}], "brand_name": "METOPROLOL SUCCINATE", "product_id": "71205-162_cc58a663-d683-41fb-bf47-1e07ffaa0fe0", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71205-162", "generic_name": "Metoprolol succinate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL SUCCINATE", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "NDA019962", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180101", "listing_expiration_date": "20261231"}