metoprolol succinate

Generic: metoprolol succinate

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

Drug Facts

Product Profile

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

metoprolol succinate 50 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7997
Product ID 68788-7997_25365bf6-6b2b-4ffe-8012-7b346c2b5fdd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203894
Listing Expiration 2026-12-31
Marketing Start 2021-08-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887997
Hyphenated Format 68788-7997

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 ANDA203894 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-1)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-3)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-6)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-9)
source: ndc

Packages (4)

68788-7997-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-1) 68788-7997-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-3) 68788-7997-6 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-6) 68788-7997-9 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-9)

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": "25365bf6-6b2b-4ffe-8012-7b346c2b5fdd", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["b8662d0c-f3c3-4331-aecb-6ba4e53785ef"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-1)", "package_ndc": "68788-7997-1", "marketing_start_date": "20210810"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-3)", "package_ndc": "68788-7997-3", "marketing_start_date": "20210810"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-6)", "package_ndc": "68788-7997-6", "marketing_start_date": "20210810"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-9)", "package_ndc": "68788-7997-9", "marketing_start_date": "20210810"}], "brand_name": "metoprolol succinate", "product_id": "68788-7997_25365bf6-6b2b-4ffe-8012-7b346c2b5fdd", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-7997", "generic_name": "metoprolol succinate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metoprolol succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA203894", "marketing_category": "ANDA", "marketing_start_date": "20210810", "listing_expiration_date": "20261231"}