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 50090-5741
Product ID 50090-5741_2a2cb20e-d82d-4dab-8a26-4be38e8d02a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078512
Listing Expiration 2026-12-31
Marketing Start 2007-10-31

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 500905741
Hyphenated Format 50090-5741

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 ANDA078512 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50090-5741-0)
  • 30 TABLET in 1 BOTTLE (50090-5741-1)
  • 60 TABLET in 1 BOTTLE (50090-5741-4)
  • 200 TABLET in 1 BOTTLE (50090-5741-7)
  • 90 TABLET in 1 BOTTLE (50090-5741-8)
source: ndc

Packages (5)

Ingredients (1)

atenolol (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a2cb20e-d82d-4dab-8a26-4be38e8d02a2", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["98471493-56ee-47a4-9120-0975c265361e"], "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 (50090-5741-0)", "package_ndc": "50090-5741-0", "marketing_start_date": "20210929"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5741-1)", "package_ndc": "50090-5741-1", "marketing_start_date": "20210929"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5741-4)", "package_ndc": "50090-5741-4", "marketing_start_date": "20210929"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (50090-5741-7)", "package_ndc": "50090-5741-7", "marketing_start_date": "20210929"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5741-8)", "package_ndc": "50090-5741-8", "marketing_start_date": "20210929"}], "brand_name": "Atenolol", "product_id": "50090-5741_2a2cb20e-d82d-4dab-8a26-4be38e8d02a2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5741", "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": "ANDA078512", "marketing_category": "ANDA", "marketing_start_date": "20071031", "listing_expiration_date": "20261231"}