atenolol

Generic: atenolol

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-229
Product ID 71205-229_b4104f4d-5d3f-4a1e-bc62-208a3c7a688e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077443
Listing Expiration 2026-12-31
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 71205229
Hyphenated Format 71205-229

Supplemental Identifiers

RxCUI
197381
UPC
0371205229306
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
  • 30 TABLET in 1 BOTTLE (71205-229-30)
  • 60 TABLET in 1 BOTTLE (71205-229-60)
  • 90 TABLET in 1 BOTTLE (71205-229-90)
source: ndc

Packages (3)

71205-229-30 30 TABLET in 1 BOTTLE (71205-229-30) 71205-229-60 60 TABLET in 1 BOTTLE (71205-229-60) 71205-229-90 90 TABLET in 1 BOTTLE (71205-229-90)

Ingredients (1)

atenolol (50 mg/1)

Linked Drug Pages (1)

Atenolol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b4104f4d-5d3f-4a1e-bc62-208a3c7a688e", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0371205229306"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["0a54656e-60dd-4ffc-b01a-423af19cd618"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-229-30)", "package_ndc": "71205-229-30", "marketing_start_date": "20190301"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-229-60)", "package_ndc": "71205-229-60", "marketing_start_date": "20190301"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-229-90)", "package_ndc": "71205-229-90", "marketing_start_date": "20190301"}], "brand_name": "Atenolol", "product_id": "71205-229_b4104f4d-5d3f-4a1e-bc62-208a3c7a688e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71205-229", "generic_name": "Atenolol", "labeler_name": "Proficient Rx LP", "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": "20261231"}