metoprolol tartrate

Generic: metoprolol tartrate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-978
Product ID 82804-978_de781298-37cb-4c03-8431-b6d86ffbde0d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074453
Listing Expiration 2026-12-31
Marketing Start 2023-11-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804978
Hyphenated Format 82804-978

Supplemental Identifiers

RxCUI
866511 866514
UPC
0382804979301 0382804978304
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 ANDA074453 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82804-978-00)
  • 1000 TABLET in 1 BOTTLE (82804-978-11)
  • 30 TABLET in 1 BOTTLE (82804-978-30)
  • 500 TABLET in 1 BOTTLE (82804-978-55)
  • 60 TABLET in 1 BOTTLE (82804-978-60)
  • 90 TABLET in 1 BOTTLE (82804-978-90)
source: ndc

Packages (6)

82804-978-00 100 TABLET in 1 BOTTLE (82804-978-00) 82804-978-11 1000 TABLET in 1 BOTTLE (82804-978-11) 82804-978-30 30 TABLET in 1 BOTTLE (82804-978-30) 82804-978-55 500 TABLET in 1 BOTTLE (82804-978-55) 82804-978-60 60 TABLET in 1 BOTTLE (82804-978-60) 82804-978-90 90 TABLET in 1 BOTTLE (82804-978-90)

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": "de781298-37cb-4c03-8431-b6d86ffbde0d", "openfda": {"upc": ["0382804979301", "0382804978304"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514"], "spl_set_id": ["de781298-37cb-4c03-8431-b6d86ffbde0d"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82804-978-00)", "package_ndc": "82804-978-00", "marketing_start_date": "20250311"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-978-11)", "package_ndc": "82804-978-11", "marketing_start_date": "20250311"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-978-30)", "package_ndc": "82804-978-30", "marketing_start_date": "20250311"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-978-55)", "package_ndc": "82804-978-55", "marketing_start_date": "20250311"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-978-60)", "package_ndc": "82804-978-60", "marketing_start_date": "20250311"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-978-90)", "package_ndc": "82804-978-90", "marketing_start_date": "20250311"}], "brand_name": "Metoprolol Tartrate", "product_id": "82804-978_de781298-37cb-4c03-8431-b6d86ffbde0d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82804-978", "generic_name": "Metoprolol Tartrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA074453", "marketing_category": "ANDA", "marketing_start_date": "20231102", "listing_expiration_date": "20261231"}