metoprolol tartrate

Generic: metoprolol tartrate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 55289-382
Product ID 55289-382_419a0b55-030b-2dbc-e063-6394a90a0cf2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076704
Listing Expiration 2026-12-31
Marketing Start 2004-02-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55289382
Hyphenated Format 55289-382

Supplemental Identifiers

RxCUI
866924
UPC
0355289382140
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 ANDA076704 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-14)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-90)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-93)
source: ndc

Packages (5)

55289-382-14 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-14) 55289-382-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-30) 55289-382-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-60) 55289-382-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-90) 55289-382-93 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-93)

Ingredients (1)

metoprolol tartrate (25 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": "419a0b55-030b-2dbc-e063-6394a90a0cf2", "openfda": {"upc": ["0355289382140"], "unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["ab44f4c5-9497-4c92-8545-e4718ddb8f08"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-14)", "package_ndc": "55289-382-14", "marketing_start_date": "20170512"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-30)", "package_ndc": "55289-382-30", "marketing_start_date": "20120502"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-60)", "package_ndc": "55289-382-60", "marketing_start_date": "20120502"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-90)", "package_ndc": "55289-382-90", "marketing_start_date": "20120502"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-382-93)", "package_ndc": "55289-382-93", "marketing_start_date": "20120502"}], "brand_name": "Metoprolol Tartrate", "product_id": "55289-382_419a0b55-030b-2dbc-e063-6394a90a0cf2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "55289-382", "generic_name": "metoprolol tartrate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA076704", "marketing_category": "ANDA", "marketing_start_date": "20040223", "listing_expiration_date": "20261231"}