metoprolol tartrate

Generic: metoprolol tartrate

Labeler: trupharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler trupharma llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 100 mg/1

Manufacturer
TruPharma LLC

Identifiers & Regulatory

Product NDC 52817-362
Product ID 52817-362_294dc99d-4a6d-22b6-e063-6394a90a06aa
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 52817362
Hyphenated Format 52817-362

Supplemental Identifiers

RxCUI
866511 866514 866924 1606347 1606349
UPC
0352817361103 0352817361004 0352817360106 0352817362100 0352817358509 0352817359506 0352817362001 0352817360007 0352817358103 0352817359100
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 ANDA200981 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (52817-362-00)
  • 100 TABLET, FILM COATED in 1 BOTTLE (52817-362-10)
source: ndc

Packages (2)

52817-362-00 1000 TABLET, FILM COATED in 1 BOTTLE (52817-362-00) 52817-362-10 100 TABLET, FILM COATED in 1 BOTTLE (52817-362-10)

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": "294dc99d-4a6d-22b6-e063-6394a90a06aa", "openfda": {"upc": ["0352817361103", "0352817361004", "0352817360106", "0352817362100", "0352817358509", "0352817359506", "0352817362001", "0352817360007", "0352817358103", "0352817359100"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924", "1606347", "1606349"], "spl_set_id": ["52c822f2-4a71-4ab2-a470-58074622846a"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (52817-362-00)", "package_ndc": "52817-362-00", "marketing_start_date": "20181201"}, {"sample": true, "description": "100 TABLET, FILM COATED in 1 BOTTLE (52817-362-10)", "package_ndc": "52817-362-10", "marketing_start_date": "20181201"}], "brand_name": "Metoprolol Tartrate", "product_id": "52817-362_294dc99d-4a6d-22b6-e063-6394a90a06aa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "52817-362", "generic_name": "Metoprolol Tartrate", "labeler_name": "TruPharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}