atenolol

Generic: atenolol

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 25 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-168
Product ID 65862-168_c5b37783-b0a1-4d21-b0cc-69a13cc4d2db
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078512
Listing Expiration 2026-12-31
Marketing Start 2007-10-31

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 65862168
Hyphenated Format 65862-168

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 ANDA078512 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (65862-168-01)
  • 1000 TABLET in 1 BOTTLE (65862-168-99)
source: ndc

Packages (2)

65862-168-01 100 TABLET in 1 BOTTLE (65862-168-01) 65862-168-99 1000 TABLET in 1 BOTTLE (65862-168-99)

Ingredients (1)

atenolol (25 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": "c5b37783-b0a1-4d21-b0cc-69a13cc4d2db", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197379", "197380", "197381"], "spl_set_id": ["1b8a4689-3916-4f4b-b54a-bbb4e322d79b"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-168-01)", "package_ndc": "65862-168-01", "marketing_start_date": "20071031"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-168-99)", "package_ndc": "65862-168-99", "marketing_start_date": "20071031"}], "brand_name": "Atenolol", "product_id": "65862-168_c5b37783-b0a1-4d21-b0cc-69a13cc4d2db", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "65862-168", "generic_name": "Atenolol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "25 mg/1"}], "application_number": "ANDA078512", "marketing_category": "ANDA", "marketing_start_date": "20071031", "listing_expiration_date": "20261231"}