metoprolol tartrate

Generic: metoprolol tartrate

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler northwind health company, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-527
Product ID 51655-527_494dd968-14a0-24ee-e063-6294a90a5108
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Listing Expiration 2027-12-31
Marketing Start 2022-09-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655527
Hyphenated Format 51655-527

Supplemental Identifiers

RxCUI
866514
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
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-25)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-26)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-52)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-83)
source: ndc

Packages (4)

51655-527-25 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-25) 51655-527-26 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-26) 51655-527-52 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-52) 51655-527-83 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-83)

Ingredients (1)

metoprolol tartrate (50 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": "494dd968-14a0-24ee-e063-6294a90a5108", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["f319e981-81ff-22da-e053-2a95a90a2738"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-25)", "package_ndc": "51655-527-25", "marketing_start_date": "20221025"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-26)", "package_ndc": "51655-527-26", "marketing_start_date": "20220916"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-52)", "package_ndc": "51655-527-52", "marketing_start_date": "20221021"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-83)", "package_ndc": "51655-527-83", "marketing_start_date": "20230328"}], "brand_name": "Metoprolol Tartrate", "product_id": "51655-527_494dd968-14a0-24ee-e063-6294a90a5108", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51655-527", "generic_name": "Metoprolol Tartrate", "labeler_name": "Northwind Health Company, LLC", "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": "20220916", "listing_expiration_date": "20271231"}