atenolol

Generic: atenolol

Labeler: ipca laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler ipca laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 100 mg/1

Manufacturer
Ipca Laboratories Limited

Identifiers & Regulatory

Product NDC 83980-024
Product ID 83980-024_d32b777e-6c64-4899-934b-4fb73d9eba85
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077877
Listing Expiration 2027-12-31
Marketing Start 2007-12-04

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 83980024
Hyphenated Format 83980-024

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 ANDA077877 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (83980-024-01)
  • 1000 TABLET in 1 BOTTLE (83980-024-10)
  • 10 TABLET in 1 BOTTLE (83980-024-97)
source: ndc

Packages (3)

83980-024-01 100 TABLET in 1 BOTTLE (83980-024-01) 83980-024-10 1000 TABLET in 1 BOTTLE (83980-024-10) 83980-024-97 10 TABLET in 1 BOTTLE (83980-024-97)

Ingredients (1)

atenolol (100 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": "d32b777e-6c64-4899-934b-4fb73d9eba85", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197379", "197380", "197381"], "spl_set_id": ["98d29958-b026-4888-a516-7bb85bb7d479"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Ipca Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (83980-024-01)", "package_ndc": "83980-024-01", "marketing_start_date": "20260130"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (83980-024-10)", "package_ndc": "83980-024-10", "marketing_start_date": "20260130"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (83980-024-97)", "package_ndc": "83980-024-97", "marketing_start_date": "20260130"}], "brand_name": "Atenolol", "product_id": "83980-024_d32b777e-6c64-4899-934b-4fb73d9eba85", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "83980-024", "generic_name": "Atenolol", "labeler_name": "Ipca Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "100 mg/1"}], "application_number": "ANDA077877", "marketing_category": "ANDA", "marketing_start_date": "20071204", "listing_expiration_date": "20271231"}