atenolol

Generic: atenolol

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler zydus pharmaceuticals usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 25 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 68382-022
Product ID 68382-022_860eb406-b330-4b72-b768-122d57c74293
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 68382022
Hyphenated Format 68382-022

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
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68382-022-01)
  • 1000 TABLET in 1 BOTTLE (68382-022-10)
  • 90 TABLET in 1 BOTTLE (68382-022-16)
  • 10000 TABLET in 1 BOTTLE (68382-022-24)
  • 5000 TABLET in 1 BOTTLE (68382-022-40)
source: ndc

Packages (5)

68382-022-01 100 TABLET in 1 BOTTLE (68382-022-01) 68382-022-10 1000 TABLET in 1 BOTTLE (68382-022-10) 68382-022-16 90 TABLET in 1 BOTTLE (68382-022-16) 68382-022-24 10000 TABLET in 1 BOTTLE (68382-022-24) 68382-022-40 5000 TABLET in 1 BOTTLE (68382-022-40)

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": "860eb406-b330-4b72-b768-122d57c74293", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197379", "197380", "197381"], "spl_set_id": ["db801706-1362-44c7-92ab-f584f96c7e1c"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-022-01)", "package_ndc": "68382-022-01", "marketing_start_date": "20051008"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-022-10)", "package_ndc": "68382-022-10", "marketing_start_date": "20051008"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68382-022-16)", "package_ndc": "68382-022-16", "marketing_start_date": "20051008"}, {"sample": false, "description": "10000 TABLET in 1 BOTTLE (68382-022-24)", "package_ndc": "68382-022-24", "marketing_start_date": "20051008"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (68382-022-40)", "package_ndc": "68382-022-40", "marketing_start_date": "20051008"}], "brand_name": "Atenolol", "product_id": "68382-022_860eb406-b330-4b72-b768-122d57c74293", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68382-022", "generic_name": "Atenolol", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "25 mg/1"}], "application_number": "ANDA076900", "marketing_category": "ANDA", "marketing_start_date": "20051008", "listing_expiration_date": "20261231"}