metoprolol tartrate

Generic: metoprolol tartrate

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 50 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-138
Product ID 71610-138_b58c8fbf-c7b3-4b9c-84a9-e19bd76904ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Listing Expiration 2026-12-31
Marketing Start 2007-09-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610138
Hyphenated Format 71610-138

Supplemental Identifiers

RxCUI
866514 866924
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
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-138-60)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71610-138-70)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71610-138-80)
  • 270 TABLET, FILM COATED in 1 BOTTLE (71610-138-92)
source: ndc

Packages (4)

71610-138-60 90 TABLET, FILM COATED in 1 BOTTLE (71610-138-60) 71610-138-70 120 TABLET, FILM COATED in 1 BOTTLE (71610-138-70) 71610-138-80 180 TABLET, FILM COATED in 1 BOTTLE (71610-138-80) 71610-138-92 270 TABLET, FILM COATED in 1 BOTTLE (71610-138-92)

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": "b58c8fbf-c7b3-4b9c-84a9-e19bd76904ac", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514", "866924"], "spl_set_id": ["b60d2cb0-f2c3-4ad5-8060-5179d5b94256"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-138-60)", "package_ndc": "71610-138-60", "marketing_start_date": "20180830"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71610-138-70)", "package_ndc": "71610-138-70", "marketing_start_date": "20180830"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71610-138-80)", "package_ndc": "71610-138-80", "marketing_start_date": "20180830"}, {"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (71610-138-92)", "package_ndc": "71610-138-92", "marketing_start_date": "20180830"}], "brand_name": "Metoprolol Tartrate", "product_id": "71610-138_b58c8fbf-c7b3-4b9c-84a9-e19bd76904ac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71610-138", "generic_name": "Metoprolol Tartrate", "labeler_name": "Aphena Pharma Solutions - Tennessee, 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": "20070911", "listing_expiration_date": "20261231"}