metoprolol tartrate

Generic: metoprolol tartrate

Labeler: advagen pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

metoprolol tartrate 100 mg/1

Manufacturer
Advagen Pharma Limited

Identifiers & Regulatory

Product NDC 72888-006
Product ID 72888-006_48450d44-3cc6-45be-e063-6394a90aac70
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2027-12-31
Marketing Start 2018-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72888006
Hyphenated Format 72888-006

Supplemental Identifiers

RxCUI
866511 866514 866924 1606347 1606349
UPC
0372888006000 0372888101057 0372888004006 0372888101019 0372888023052 0372888006017 0372888006055 0372888023014 0372888005058 0372888004013 0372888005003 0372888005010 0372888004051
UNII
W5S57Y3A5L

Packaging Origin

Original Packager
true

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
  • 1000 TABLET, FILM COATED in 1 BOTTLE (72888-006-00)
  • 100 TABLET, FILM COATED in 1 BOTTLE (72888-006-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (72888-006-05)
source: ndc

Packages (3)

72888-006-00 1000 TABLET, FILM COATED in 1 BOTTLE (72888-006-00) 72888-006-01 100 TABLET, FILM COATED in 1 BOTTLE (72888-006-01) 72888-006-05 500 TABLET, FILM COATED in 1 BOTTLE (72888-006-05)

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": "48450d44-3cc6-45be-e063-6394a90aac70", "openfda": {"upc": ["0372888006000", "0372888101057", "0372888004006", "0372888101019", "0372888023052", "0372888006017", "0372888006055", "0372888023014", "0372888005058", "0372888004013", "0372888005003", "0372888005010", "0372888004051"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511", "866514", "866924", "1606347", "1606349"], "spl_set_id": ["a401fe31-d51a-49d9-a062-c9d22088db56"], "manufacturer_name": ["Advagen Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72888-006-00)", "package_ndc": "72888-006-00", "marketing_start_date": "20241018"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72888-006-01)", "package_ndc": "72888-006-01", "marketing_start_date": "20241018"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72888-006-05)", "package_ndc": "72888-006-05", "marketing_start_date": "20241018"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "72888-006_48450d44-3cc6-45be-e063-6394a90aac70", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72888-006", "generic_name": "METOPROLOL TARTRATE", "labeler_name": "Advagen Pharma Limited", "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": "20181201", "listing_expiration_date": "20271231"}