metoprolol succinate

Generic: metoprolol succinate

Labeler: nivagen pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol succinate
Generic Name metoprolol succinate
Labeler nivagen pharmaceuticals, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metoprolol succinate 25 mg/1

Manufacturer
Nivagen Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 75834-290
Product ID 75834-290_0175a6b8-51dd-44d3-e063-6394a90a2f03
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203028
Listing Expiration 2026-12-31
Marketing Start 2021-02-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 75834290
Hyphenated Format 75834-290

Supplemental Identifiers

RxCUI
866427 866436
UPC
0375834290010 0375834291017 0375834291055 0375834290058 0375834290003 0375834291000
UNII
TH25PD4CCB

Packaging Origin

Original Packager
true

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 ANDA203028 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-00)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-05)
source: ndc

Packages (3)

75834-290-00 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-00) 75834-290-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-01) 75834-290-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-05)

Ingredients (1)

metoprolol succinate (25 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": "0175a6b8-51dd-44d3-e063-6394a90a2f03", "openfda": {"upc": ["0375834290010", "0375834291017", "0375834291055", "0375834290058", "0375834290003", "0375834291000"], "unii": ["TH25PD4CCB"], "rxcui": ["866427", "866436"], "spl_set_id": ["da7a5fcc-1794-e118-e053-2a95a90a25c3"], "manufacturer_name": ["Nivagen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-00)", "package_ndc": "75834-290-00", "marketing_start_date": "20220223"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-01)", "package_ndc": "75834-290-01", "marketing_start_date": "20220223"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-290-05)", "package_ndc": "75834-290-05", "marketing_start_date": "20220223"}], "brand_name": "Metoprolol Succinate", "product_id": "75834-290_0175a6b8-51dd-44d3-e063-6394a90a2f03", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "75834-290", "generic_name": "Metoprolol Succinate", "labeler_name": "Nivagen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA203028", "marketing_category": "ANDA", "marketing_start_date": "20210226", "listing_expiration_date": "20261231"}