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 tartrate 100 mg/1

Manufacturer
Preferred Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 68788-8448
Product ID 68788-8448_8391e0b0-230f-4cd0-ac34-c8127ad16349
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207206
Listing Expiration 2026-12-31
Marketing Start 2023-05-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888448
Hyphenated Format 68788-8448

Supplemental Identifiers

RxCUI
866412
UNII
W5S57Y3A5L

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 ANDA207206 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-1)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-3)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-6)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-9)
source: ndc

Packages (4)

68788-8448-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-1) 68788-8448-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-3) 68788-8448-6 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-6) 68788-8448-9 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-9)

Ingredients (1)

metoprolol tartrate (100 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": "8391e0b0-230f-4cd0-ac34-c8127ad16349", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866412"], "spl_set_id": ["0ded3105-b962-4748-bf5b-fca7a4557562"], "manufacturer_name": ["Preferred Pharmaceuticals Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-1)", "package_ndc": "68788-8448-1", "marketing_start_date": "20230515"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-3)", "package_ndc": "68788-8448-3", "marketing_start_date": "20230515"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-6)", "package_ndc": "68788-8448-6", "marketing_start_date": "20230515"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8448-9)", "package_ndc": "68788-8448-9", "marketing_start_date": "20230515"}], "brand_name": "Metoprolol Succinate", "product_id": "68788-8448_8391e0b0-230f-4cd0-ac34-c8127ad16349", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-8448", "generic_name": "Metoprolol Succinate", "labeler_name": "Preferred Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA207206", "marketing_category": "ANDA", "marketing_start_date": "20230515", "listing_expiration_date": "20261231"}