metoprolol tartrate

Generic: metoprolol tartrate

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 37.5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-758
Product ID 59651-758_2d3b41ae-f657-4459-bdee-e76e644ec167
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Listing Expiration 2026-12-31
Marketing Start 2023-12-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651758
Hyphenated Format 59651-758

Supplemental Identifiers

RxCUI
1606347 1606349
UPC
0359651760017 0359651758014
UNII
W5S57Y3A5L

Packaging Origin

Original Packager
true

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 ANDA077739 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59651-758-01)
source: ndc

Packages (1)

59651-758-01 100 TABLET, FILM COATED in 1 BOTTLE (59651-758-01)

Ingredients (1)

metoprolol tartrate (37.5 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": "2d3b41ae-f657-4459-bdee-e76e644ec167", "openfda": {"upc": ["0359651760017", "0359651758014"], "unii": ["W5S57Y3A5L"], "rxcui": ["1606347", "1606349"], "spl_set_id": ["ac4ac150-d3e6-4bd1-8a4a-7d63fade3e49"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-758-01)", "package_ndc": "59651-758-01", "marketing_start_date": "20231207"}], "brand_name": "Metoprolol Tartrate", "product_id": "59651-758_2d3b41ae-f657-4459-bdee-e76e644ec167", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "59651-758", "generic_name": "Metoprolol Tartrate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "37.5 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20231207", "listing_expiration_date": "20261231"}