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
Routes
ORAL
Active Ingredients

metoprolol tartrate 100 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-659
Product ID 72189-659_499ce022-12a8-e4e5-e063-6394a90a435a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2027-12-31
Marketing Start 2026-01-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189659
Hyphenated Format 72189-659

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
  • 90 TABLET in 1 BOTTLE (72189-659-90)
source: ndc

Packages (1)

72189-659-90 90 TABLET in 1 BOTTLE (72189-659-90)

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": "499ce022-12a8-e4e5-e063-6394a90a435a", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["499ce022-12a7-e4e5-e063-6394a90a435a"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-659-90)", "package_ndc": "72189-659-90", "marketing_start_date": "20260130"}], "brand_name": "Metoprolol Tartrate", "product_id": "72189-659_499ce022-12a8-e4e5-e063-6394a90a435a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-659", "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": "20260130", "listing_expiration_date": "20271231"}