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 50090-5367
Product ID 50090-5367_b1954c6b-552e-4621-942a-a65d99eef297
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077443
Listing Expiration 2027-12-31
Marketing Start 2010-06-10

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 500905367
Hyphenated Format 50090-5367

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 ANDA077443 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50090-5367-0)
  • 30 TABLET in 1 BOTTLE (50090-5367-1)
  • 200 TABLET in 1 BOTTLE (50090-5367-7)
  • 90 TABLET in 1 BOTTLE (50090-5367-8)
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": "b1954c6b-552e-4621-942a-a65d99eef297", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["e4ece8f4-3714-42ba-b36d-d00586dfd33a"], "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 (50090-5367-0)", "package_ndc": "50090-5367-0", "marketing_start_date": "20201118"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5367-1)", "package_ndc": "50090-5367-1", "marketing_start_date": "20201118"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (50090-5367-7)", "package_ndc": "50090-5367-7", "marketing_start_date": "20201118"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5367-8)", "package_ndc": "50090-5367-8", "marketing_start_date": "20201118"}], "brand_name": "Atenolol", "product_id": "50090-5367_b1954c6b-552e-4621-942a-a65d99eef297", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5367", "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": "ANDA077443", "marketing_category": "ANDA", "marketing_start_date": "20100610", "listing_expiration_date": "20271231"}