metoprolol succinate
Generic: metoprolol succinate
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
metoprolol succinate
Generic Name
metoprolol succinate
Labeler
direct_rx
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metoprolol succinate 100 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61919334
Hyphenated Format
61919-334
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 (source: ndc)
Application Number
ANDA078889 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-334-30)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-334-90)
Packages (2)
Ingredients (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"}