metoprolol succinate

Generic: metoprolol succinate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

metoprolol succinate 25 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0158
Product ID 71335-0158_609cf08a-a8d7-4e20-83e6-05823fb89286
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090617
Listing Expiration 2026-12-31
Marketing Start 2012-09-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350158
Hyphenated Format 71335-0158

Supplemental Identifiers

RxCUI
866427 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 ANDA090617 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-1)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-2)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-3)
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-4)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-5)
source: ndc

Packages (5)

71335-0158-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-1) 71335-0158-2 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-2) 71335-0158-3 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-3) 71335-0158-4 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-4) 71335-0158-5 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-5)

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": "609cf08a-a8d7-4e20-83e6-05823fb89286", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427", "866436"], "spl_set_id": ["42bb324d-8b1e-45db-b15e-3845eec83c38"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-1)", "package_ndc": "71335-0158-1", "marketing_start_date": "20130627"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-2)", "package_ndc": "71335-0158-2", "marketing_start_date": "20130627"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-3)", "package_ndc": "71335-0158-3", "marketing_start_date": "20130627"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-4)", "package_ndc": "71335-0158-4", "marketing_start_date": "20130627"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-5)", "package_ndc": "71335-0158-5", "marketing_start_date": "20130627"}], "brand_name": "Metoprolol succinate", "product_id": "71335-0158_609cf08a-a8d7-4e20-83e6-05823fb89286", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-0158", "generic_name": "Metoprolol succinate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA090617", "marketing_category": "ANDA", "marketing_start_date": "20120910", "listing_expiration_date": "20261231"}