tenormin

Generic: atenolol

Labeler: almatica pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name tenormin
Generic Name atenolol
Labeler almatica pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
Almatica Pharma LLC

Identifiers & Regulatory

Product NDC 52427-430
Product ID 52427-430_ecd0de7b-801e-a5d6-01b7-01b89a8f3a78
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018240
Marketing Start 2015-04-15
Marketing End 2026-09-30

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 52427430
Hyphenated Format 52427-430

Supplemental Identifiers

RxCUI
150750 152414 197379 197380 197381 201322
UPC
0352427431906 0352427430909 0352427429903
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 (52427-430-90)
source: ndc

Packages (1)

52427-430-90 90 TABLET in 1 BOTTLE (52427-430-90)

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": "ecd0de7b-801e-a5d6-01b7-01b89a8f3a78", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0352427431906", "0352427430909", "0352427429903"], "unii": ["50VV3VW0TI"], "rxcui": ["150750", "152414", "197379", "197380", "197381", "201322"], "spl_set_id": ["746db603-a6e1-4dc3-c2d8-92314419098c"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Almatica Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (52427-430-90)", "package_ndc": "52427-430-90", "marketing_end_date": "20260930", "marketing_start_date": "20150415"}], "brand_name": "TENORMIN", "product_id": "52427-430_ecd0de7b-801e-a5d6-01b7-01b89a8f3a78", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "52427-430", "generic_name": "Atenolol", "labeler_name": "Almatica Pharma 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_end_date": "20260930", "marketing_start_date": "20150415"}