atenolol
Generic: atenolol
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
atenolol
Generic Name
atenolol
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
atenolol 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4099
Product ID
70518-4099_3fa4626e-9630-92f5-e063-6294a90afb12
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078512
Listing Expiration
2026-12-31
Marketing Start
2024-06-12
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184099
Hyphenated Format
70518-4099
Supplemental Identifiers
RxCUI
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
ANDA078512 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-4099-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fa4626e-9630-92f5-e063-6294a90afb12", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197379"], "spl_set_id": ["cdca0ef8-2ac3-4430-a662-f88522f68d8e"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4099-0)", "package_ndc": "70518-4099-0", "marketing_start_date": "20240612"}], "brand_name": "Atenolol", "product_id": "70518-4099_3fa4626e-9630-92f5-e063-6294a90afb12", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4099", "generic_name": "Atenolol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "100 mg/1"}], "application_number": "ANDA078512", "marketing_category": "ANDA", "marketing_start_date": "20240612", "listing_expiration_date": "20261231"}