atenolol

Generic: atenolol

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 65841-023
Product ID 65841-023_f4fb6b85-6379-4e8a-9ee3-402819d128a0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076900
Listing Expiration 2026-12-31
Marketing Start 2005-10-08

Pharmacologic Class

Established (EPC)
beta-adrenergic blocker [epc]
Mechanism of Action
adrenergic beta-antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65841023
Hyphenated Format 65841-023

Supplemental Identifiers

RxCUI
197379 197380 197381
UNII
50VV3VW0TI
NUI
N0000000161 N0000175556

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 atenolol (source: ndc)
Generic Name atenolol (source: ndc)
Application Number ANDA076900 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (65841-023-01)
  • 2000 TABLET in 1 BOTTLE (65841-023-02)
  • 1000 TABLET in 1 BOTTLE (65841-023-10)
  • 90 TABLET in 1 BOTTLE (65841-023-16)
  • 10000 TABLET in 1 BOTTLE (65841-023-24)
  • 5000 TABLET in 1 BOTTLE (65841-023-40)
source: ndc

Packages (6)

65841-023-01 100 TABLET in 1 BOTTLE (65841-023-01) 65841-023-02 2000 TABLET in 1 BOTTLE (65841-023-02) 65841-023-10 1000 TABLET in 1 BOTTLE (65841-023-10) 65841-023-16 90 TABLET in 1 BOTTLE (65841-023-16) 65841-023-24 10000 TABLET in 1 BOTTLE (65841-023-24) 65841-023-40 5000 TABLET in 1 BOTTLE (65841-023-40)

Ingredients (1)

atenolol (50 mg/1)

Linked Drug Pages (1)

Atenolol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f4fb6b85-6379-4e8a-9ee3-402819d128a0", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197379", "197380", "197381"], "spl_set_id": ["2492d5f6-00b0-42c9-a793-2be83ea81ad1"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65841-023-01)", "package_ndc": "65841-023-01", "marketing_start_date": "20051008"}, {"sample": false, "description": "2000 TABLET in 1 BOTTLE (65841-023-02)", "package_ndc": "65841-023-02", "marketing_start_date": "20051008"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65841-023-10)", "package_ndc": "65841-023-10", "marketing_start_date": "20051008"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65841-023-16)", "package_ndc": "65841-023-16", "marketing_start_date": "20051008"}, {"sample": false, "description": "10000 TABLET in 1 BOTTLE (65841-023-24)", "package_ndc": "65841-023-24", "marketing_start_date": "20051008"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (65841-023-40)", "package_ndc": "65841-023-40", "marketing_start_date": "20051008"}], "brand_name": "Atenolol", "product_id": "65841-023_f4fb6b85-6379-4e8a-9ee3-402819d128a0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "65841-023", "generic_name": "Atenolol", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}], "application_number": "ANDA076900", "marketing_category": "ANDA", "marketing_start_date": "20051008", "listing_expiration_date": "20261231"}