metoprolol tartrate

Generic: metoprolol

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metoprolol tartrate 25 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-003
Product ID 71205-003_56227d4b-1b33-412c-9dee-e421fc0d82fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202871
Listing Expiration 2026-12-31
Marketing Start 2016-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205003
Hyphenated Format 71205-003

Supplemental Identifiers

RxCUI
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 (source: ndc)
Application Number ANDA202871 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-003-30)
  • 60 TABLET in 1 BOTTLE (71205-003-60)
  • 180 TABLET in 1 BOTTLE (71205-003-78)
  • 90 TABLET in 1 BOTTLE (71205-003-90)
source: ndc

Packages (4)

Ingredients (1)

metoprolol tartrate (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "56227d4b-1b33-412c-9dee-e421fc0d82fc", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["95b95aab-0733-4189-b4c0-429a1046c534"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-003-30)", "package_ndc": "71205-003-30", "marketing_start_date": "20180402"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-003-60)", "package_ndc": "71205-003-60", "marketing_start_date": "20180402"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71205-003-78)", "package_ndc": "71205-003-78", "marketing_start_date": "20180402"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-003-90)", "package_ndc": "71205-003-90", "marketing_start_date": "20180402"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "71205-003_56227d4b-1b33-412c-9dee-e421fc0d82fc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71205-003", "generic_name": "METOPROLOL", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA202871", "marketing_category": "ANDA", "marketing_start_date": "20160731", "listing_expiration_date": "20261231"}