metoprolol tartrate

Generic: metoprolol tartrate

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

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7548
Product ID 68788-7548_fe23ccc4-a2eb-4414-960e-35836e730c15
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2026-12-31
Marketing Start 2018-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887548
Hyphenated Format 68788-7548

Supplemental Identifiers

RxCUI
866514
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 tartrate (source: ndc)
Generic Name metoprolol tartrate (source: ndc)
Application Number ANDA200981 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-7548-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7548-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-7548-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-7548-9)
source: ndc

Packages (4)

68788-7548-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7548-1) 68788-7548-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7548-3) 68788-7548-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-7548-6) 68788-7548-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-7548-9)

Ingredients (1)

metoprolol tartrate (50 mg/1)

Linked Drug Pages (1)

Metoprolol Tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fe23ccc4-a2eb-4414-960e-35836e730c15", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["b4d1e5ba-f1a8-4c77-bd65-db8e9342370b"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-7548-1)", "package_ndc": "68788-7548-1", "marketing_start_date": "20191227"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7548-3)", "package_ndc": "68788-7548-3", "marketing_start_date": "20191227"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7548-6)", "package_ndc": "68788-7548-6", "marketing_start_date": "20191227"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7548-9)", "package_ndc": "68788-7548-9", "marketing_start_date": "20191227"}], "brand_name": "Metoprolol Tartrate", "product_id": "68788-7548_fe23ccc4-a2eb-4414-960e-35836e730c15", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-7548", "generic_name": "Metoprolol Tartrate", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}