metoprolol tartrate

Generic: metoprolol tartrate

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

metoprolol tartrate 100 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-544
Product ID 72189-544_4c4a8de0-6464-8c06-e063-6394a90aeea9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2027-12-31
Marketing Start 2024-03-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189544
Hyphenated Format 72189-544

Supplemental Identifiers

RxCUI
866511
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 ANDA200981 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-544-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (72189-544-90)
source: ndc

Packages (2)

72189-544-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-544-30) 72189-544-90 90 TABLET, FILM COATED in 1 BOTTLE (72189-544-90)

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": "4c4a8de0-6464-8c06-e063-6394a90aeea9", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["13b7404f-e16b-5d43-e063-6394a90a3fca"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-544-30)", "package_ndc": "72189-544-30", "marketing_start_date": "20240315"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-544-90)", "package_ndc": "72189-544-90", "marketing_start_date": "20240315"}], "brand_name": "Metoprolol Tartrate", "product_id": "72189-544_4c4a8de0-6464-8c06-e063-6394a90aeea9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-544", "generic_name": "Metoprolol Tartrate", "labeler_name": "Direct_Rx", "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": "20240315", "listing_expiration_date": "20271231"}