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 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-532
Product ID 63187-532_7fdd60d2-87b1-4ad7-9981-a6e26806c974
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 63187532
Hyphenated Format 63187-532

Supplemental Identifiers

RxCUI
866511
UPC
0363187532307
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
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (63187-532-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (63187-532-60)
  • 120 TABLET, FILM COATED in 1 BOTTLE (63187-532-72)
  • 180 TABLET, FILM COATED in 1 BOTTLE (63187-532-78)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63187-532-90)
source: ndc

Packages (5)

63187-532-30 30 TABLET, FILM COATED in 1 BOTTLE (63187-532-30) 63187-532-60 60 TABLET, FILM COATED in 1 BOTTLE (63187-532-60) 63187-532-72 120 TABLET, FILM COATED in 1 BOTTLE (63187-532-72) 63187-532-78 180 TABLET, FILM COATED in 1 BOTTLE (63187-532-78) 63187-532-90 90 TABLET, FILM COATED in 1 BOTTLE (63187-532-90)

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": "7fdd60d2-87b1-4ad7-9981-a6e26806c974", "openfda": {"upc": ["0363187532307"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["c5c8ca26-d3dd-46ba-bf04-6aae9f334445"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-532-30)", "package_ndc": "63187-532-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-532-60)", "package_ndc": "63187-532-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (63187-532-72)", "package_ndc": "63187-532-72", "marketing_start_date": "20181201"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (63187-532-78)", "package_ndc": "63187-532-78", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-532-90)", "package_ndc": "63187-532-90", "marketing_start_date": "20181201"}], "brand_name": "Metoprolol Tartrate", "product_id": "63187-532_7fdd60d2-87b1-4ad7-9981-a6e26806c974", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63187-532", "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": "100 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}