atenolol

Generic: atenolol

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4287
Product ID 70518-4287_401bb1aa-2156-6a9d-e063-6294a90ae125
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213136
Listing Expiration 2026-12-31
Marketing Start 2025-02-12

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 705184287
Hyphenated Format 70518-4287

Supplemental Identifiers

RxCUI
197380
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 ANDA213136 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-4287-0)
source: ndc

Packages (1)

70518-4287-0 30 TABLET in 1 BLISTER PACK (70518-4287-0)

Ingredients (1)

atenolol (25 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": "401bb1aa-2156-6a9d-e063-6294a90ae125", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197380"], "spl_set_id": ["897e18f6-3b57-4ef0-85ff-9dfa23521eb9"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4287-0)", "package_ndc": "70518-4287-0", "marketing_start_date": "20250212"}], "brand_name": "Atenolol", "product_id": "70518-4287_401bb1aa-2156-6a9d-e063-6294a90ae125", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4287", "generic_name": "Atenolol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "25 mg/1"}], "application_number": "ANDA213136", "marketing_category": "ANDA", "marketing_start_date": "20250212", "listing_expiration_date": "20261231"}