metoprolol succinate

Generic: metoprolol succinate

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

metoprolol succinate 100 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 61919-334
Product ID 61919-334_0e884df8-756d-2374-e063-6394a90ab34a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078889
Listing Expiration 2026-12-31
Marketing Start 2021-01-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61919334
Hyphenated Format 61919-334

Supplemental Identifiers

RxCUI
866412 866924
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 ANDA078889 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-334-30)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-334-90)
source: ndc

Packages (2)

Ingredients (1)

metoprolol succinate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e884df8-756d-2374-e063-6394a90ab34a", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412", "866924"], "spl_set_id": ["90a69a79-5517-0ccf-e053-2995a90a441f"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-334-30)", "package_ndc": "61919-334-30", "marketing_start_date": "20210119"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-334-90)", "package_ndc": "61919-334-90", "marketing_start_date": "20210119"}], "brand_name": "METOPROLOL SUCCINATE", "product_id": "61919-334_0e884df8-756d-2374-e063-6394a90ab34a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "61919-334", "generic_name": "METOPROLOL SUCCINATE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL SUCCINATE", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078889", "marketing_category": "ANDA", "marketing_start_date": "20210119", "listing_expiration_date": "20261231"}