tenormin

Generic: atenolol

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name tenormin
Generic Name atenolol
Labeler upsher-smith laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-245
Product ID 24979-245_441e1224-9c12-4cbb-8066-01747470222e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018240
Listing Expiration 2026-12-31
Marketing Start 2024-08-01

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 24979245
Hyphenated Format 24979-245

Supplemental Identifiers

RxCUI
150750 152414 197379 197380 197381 201322
UPC
0324979246079 0324979245072 0324979244075
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 tenormin (source: ndc)
Generic Name atenolol (source: ndc)
Application Number NDA018240 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (24979-245-07)
source: ndc

Packages (1)

24979-245-07 90 TABLET in 1 BOTTLE (24979-245-07)

Ingredients (1)

atenolol (50 mg/1)

Linked Drug Pages (1)

TENORMIN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "441e1224-9c12-4cbb-8066-01747470222e", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0324979246079", "0324979245072", "0324979244075"], "unii": ["50VV3VW0TI"], "rxcui": ["150750", "152414", "197379", "197380", "197381", "201322"], "spl_set_id": ["6e850b1e-28a4-4ff8-8ed7-bb0b29faa28a"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (24979-245-07)", "package_ndc": "24979-245-07", "marketing_start_date": "20240801"}], "brand_name": "TENORMIN", "product_id": "24979-245_441e1224-9c12-4cbb-8066-01747470222e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "24979-245", "generic_name": "Atenolol", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TENORMIN", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}], "application_number": "NDA018240", "marketing_category": "NDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}