atenolol

Generic: atenolol

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-765
Product ID 43063-765_414b8e3f-9bc8-52f4-e063-6294a90a0eb3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074056
Listing Expiration 2026-12-31
Marketing Start 1995-02-22

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 43063765
Hyphenated Format 43063-765

Supplemental Identifiers

RxCUI
197381
UPC
0343063765906
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 ANDA074056 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-765-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-765-90)
source: ndc

Packages (2)

Ingredients (1)

atenolol (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "414b8e3f-9bc8-52f4-e063-6294a90a0eb3", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0343063765906"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["c69b8e5e-c7c3-4883-9cea-f7f435a8ede8"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-765-30)", "package_ndc": "43063-765-30", "marketing_start_date": "20170511"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-765-90)", "package_ndc": "43063-765-90", "marketing_start_date": "20171218"}], "brand_name": "Atenolol", "product_id": "43063-765_414b8e3f-9bc8-52f4-e063-6294a90a0eb3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43063-765", "generic_name": "Atenolol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}], "application_number": "ANDA074056", "marketing_category": "ANDA", "marketing_start_date": "19950222", "listing_expiration_date": "20261231"}