atenolol

Generic: atenolol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5363
Product ID 50090-5363_7c899e6b-8077-4970-93cb-ff9b374beef9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213136
Listing Expiration 2026-12-31
Marketing Start 2019-11-21

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 500905363
Hyphenated Format 50090-5363

Supplemental Identifiers

RxCUI
197381
UNII
50VV3VW0TI
NUI
N0000000161 N0000175556

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 ANDA213136 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50090-5363-0)
  • 30 TABLET in 1 BOTTLE (50090-5363-1)
  • 200 TABLET in 1 BOTTLE (50090-5363-7)
  • 90 TABLET in 1 BOTTLE (50090-5363-8)
source: ndc

Packages (4)

Ingredients (1)

atenolol (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7c899e6b-8077-4970-93cb-ff9b374beef9", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["d3e72119-e3c3-41ba-8787-acc86b44d6c4"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-5363-0)", "package_ndc": "50090-5363-0", "marketing_start_date": "20201117"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5363-1)", "package_ndc": "50090-5363-1", "marketing_start_date": "20221019"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (50090-5363-7)", "package_ndc": "50090-5363-7", "marketing_start_date": "20201117"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5363-8)", "package_ndc": "50090-5363-8", "marketing_start_date": "20201117"}], "brand_name": "Atenolol", "product_id": "50090-5363_7c899e6b-8077-4970-93cb-ff9b374beef9", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5363", "generic_name": "Atenolol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}], "application_number": "ANDA213136", "marketing_category": "ANDA", "marketing_start_date": "20191121", "listing_expiration_date": "20261231"}