metoprolol tartrate

Generic: metoprolol tartrate

Labeler: redpharm drug, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

metoprolol tartrate 25 mg/1

Manufacturer
RedPharm Drug, Inc

Identifiers & Regulatory

Product NDC 67296-1903
Product ID 67296-1903_2c641265-66de-dc3f-e063-6394a90a5a55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200981
Listing Expiration 2026-12-31
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 672961903
Hyphenated Format 67296-1903

Supplemental Identifiers

RxCUI
866924
UPC
0372888005010 0372888005003 0372888004013 0372888006017 0372888101057 0372888023052 0372888005058 0372888006000 0372888004006 0372888101019 0372888023014 0372888004051
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
  • 25 mg/1
source: ndc
Packaging
  • 180 TABLET, FILM COATED in 1 BOTTLE (67296-1903-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (67296-1903-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (67296-1903-9)
source: ndc

Packages (3)

67296-1903-1 180 TABLET, FILM COATED in 1 BOTTLE (67296-1903-1) 67296-1903-3 30 TABLET, FILM COATED in 1 BOTTLE (67296-1903-3) 67296-1903-9 90 TABLET, FILM COATED in 1 BOTTLE (67296-1903-9)

Ingredients (1)

metoprolol tartrate (25 mg/1)

Linked Drug Pages (2)

Metoprolol Tartrate ndc-match (0.9) Metoprolol Tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c641265-66de-dc3f-e063-6394a90a5a55", "openfda": {"upc": ["0372888005010", "0372888005003", "0372888004013", "0372888006017", "0372888101057", "0372888023052", "0372888005058", "0372888006000", "0372888004006", "0372888101019", "0372888023014", "0372888004051"], "unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["09d23356-ddf9-4dbd-e063-6394a90a217a"], "manufacturer_name": ["RedPharm Drug, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (67296-1903-1)", "package_ndc": "67296-1903-1", "marketing_start_date": "20181201"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-1903-3)", "package_ndc": "67296-1903-3", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (67296-1903-9)", "package_ndc": "67296-1903-9", "marketing_start_date": "20181201"}], "brand_name": "Metoprolol Tartrate", "product_id": "67296-1903_2c641265-66de-dc3f-e063-6394a90a5a55", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67296-1903", "generic_name": "Metoprolol Tartrate", "labeler_name": "RedPharm Drug, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}