atenolol
Generic: atenolol
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
atenolol
Generic Name
atenolol
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
atenolol 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-4553
Product ID
68071-4553_1a916209-69cf-88d0-e063-6294a90aff61
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680714553
Hyphenated Format
68071-4553
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (68071-4553-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a916209-69cf-88d0-e063-6294a90aff61", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0368071455311"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["754a1ea1-1233-066f-e053-2991aa0a33a9"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-4553-1)", "package_ndc": "68071-4553-1", "marketing_start_date": "20180907"}], "brand_name": "Atenolol", "product_id": "68071-4553_1a916209-69cf-88d0-e063-6294a90aff61", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-4553", "generic_name": "Atenolol", "labeler_name": "NuCare Pharmaceuticals,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"}