metoprolol tartrate

Generic: metoprolol tartrate

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 100 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-559
Product ID 71610-559_4b804930-cb3d-41eb-b76f-afaff44ba395
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076704
Listing Expiration 2026-12-31
Marketing Start 2004-01-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610559
Hyphenated Format 71610-559

Supplemental Identifiers

RxCUI
866511 866514 866924
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 ANDA076704 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-53)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-60)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-80)
source: ndc

Packages (3)

71610-559-53 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-53) 71610-559-60 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-60) 71610-559-80 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-80)

Ingredients (1)

metoprolol tartrate (100 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": "4b804930-cb3d-41eb-b76f-afaff44ba395", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924"], "spl_set_id": ["ea141b60-b08e-4f0f-9f29-cd765f4d7ca6"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-53)", "package_ndc": "71610-559-53", "marketing_start_date": "20210520"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-60)", "package_ndc": "71610-559-60", "marketing_start_date": "20210520"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-559-80)", "package_ndc": "71610-559-80", "marketing_start_date": "20210520"}], "brand_name": "Metoprolol Tartrate", "product_id": "71610-559_4b804930-cb3d-41eb-b76f-afaff44ba395", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71610-559", "generic_name": "metoprolol tartrate", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA076704", "marketing_category": "ANDA", "marketing_start_date": "20040116", "listing_expiration_date": "20261231"}