atenolol

Generic: atenolol

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-438
Product ID 64980-438_7bf7d854-7736-4159-81e0-2f9f0c12d73c
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 64980438
Hyphenated Format 64980-438

Supplemental Identifiers

RxCUI
197379 197380 197381
UPC
0364980437011 0364980437103 0364980438100 0364980438018 0364980439015 0364980439107
UNII
50VV3VW0TI
NUI
N0000000161 N0000175556

Packaging Origin

Original Packager
true

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 (64980-438-01)
  • 1000 TABLET in 1 BOTTLE (64980-438-10)
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": "7bf7d854-7736-4159-81e0-2f9f0c12d73c", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0364980437011", "0364980437103", "0364980438100", "0364980438018", "0364980439015", "0364980439107"], "unii": ["50VV3VW0TI"], "rxcui": ["197379", "197380", "197381"], "spl_set_id": ["96dd038f-b363-4e24-9c67-82b7c85c3bc4"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-438-01)", "package_ndc": "64980-438-01", "marketing_start_date": "20100610"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (64980-438-10)", "package_ndc": "64980-438-10", "marketing_start_date": "20100610"}], "brand_name": "Atenolol", "product_id": "64980-438_7bf7d854-7736-4159-81e0-2f9f0c12d73c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "64980-438", "generic_name": "Atenolol", "labeler_name": "Rising Pharma Holdings, Inc.", "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"}