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, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-609
Product ID 63187-609_a5cdde79-e69c-49ab-bdf6-31224a110e38
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 63187609
Hyphenated Format 63187-609

Supplemental Identifiers

RxCUI
866514
UPC
0363187609900
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 ANDA077739 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (63187-609-00)
  • 30 TABLET, FILM COATED in 1 BOTTLE (63187-609-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (63187-609-60)
  • 120 TABLET, FILM COATED in 1 BOTTLE (63187-609-72)
  • 180 TABLET, FILM COATED in 1 BOTTLE (63187-609-78)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63187-609-90)
source: ndc

Packages (6)

Ingredients (1)

metoprolol tartrate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a5cdde79-e69c-49ab-bdf6-31224a110e38", "openfda": {"upc": ["0363187609900"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["d4c8f068-7410-4543-9a66-7f4c19ff63a5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (63187-609-00)", "package_ndc": "63187-609-00", "marketing_start_date": "20181201"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-609-30)", "package_ndc": "63187-609-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-609-60)", "package_ndc": "63187-609-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (63187-609-72)", "package_ndc": "63187-609-72", "marketing_start_date": "20181201"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (63187-609-78)", "package_ndc": "63187-609-78", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-609-90)", "package_ndc": "63187-609-90", "marketing_start_date": "20181201"}], "brand_name": "Metoprolol Tartrate", "product_id": "63187-609_a5cdde79-e69c-49ab-bdf6-31224a110e38", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63187-609", "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": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}