metoprolol tartrate

Generic: metoprolol tartrate

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler rising pharma holdings, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 100 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 57237-102
Product ID 57237-102_a688acb3-72c6-4fcf-b225-648ae694279f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Listing Expiration 2026-12-31
Marketing Start 2007-09-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57237102
Hyphenated Format 57237-102

Supplemental Identifiers

RxCUI
866511 866514 866924
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
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (57237-102-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (57237-102-99)
source: ndc

Packages (2)

57237-102-01 100 TABLET, FILM COATED in 1 BOTTLE (57237-102-01) 57237-102-99 1000 TABLET, FILM COATED in 1 BOTTLE (57237-102-99)

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": "a688acb3-72c6-4fcf-b225-648ae694279f", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924"], "spl_set_id": ["30b2b576-4939-4903-be59-dbd1624a5eb6"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (57237-102-01)", "package_ndc": "57237-102-01", "marketing_start_date": "20070911"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (57237-102-99)", "package_ndc": "57237-102-99", "marketing_start_date": "20070911"}], "brand_name": "Metoprolol Tartrate", "product_id": "57237-102_a688acb3-72c6-4fcf-b225-648ae694279f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "57237-102", "generic_name": "Metoprolol Tartrate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}