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 50 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3036
Product ID 70518-3036_4b07663b-fc4b-4cad-e063-6294a90a1a8e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078512
Listing Expiration 2027-12-31
Marketing Start 2021-03-03

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 705183036
Hyphenated Format 70518-3036

Supplemental Identifiers

RxCUI
197381
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 ANDA078512 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-3036-0)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-3036-1)
source: ndc

Packages (2)

70518-3036-0 30 TABLET in 1 BLISTER PACK (70518-3036-0) 70518-3036-1 90 TABLET in 1 BOTTLE, PLASTIC (70518-3036-1)

Ingredients (1)

atenolol (50 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": "4b07663b-fc4b-4cad-e063-6294a90a1a8e", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["4ca8dd77-cdac-41fe-a742-b1b32551203b"], "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 (70518-3036-0)", "package_ndc": "70518-3036-0", "marketing_start_date": "20210303"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3036-1)", "package_ndc": "70518-3036-1", "marketing_start_date": "20210312"}], "brand_name": "Atenolol", "product_id": "70518-3036_4b07663b-fc4b-4cad-e063-6294a90a1a8e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3036", "generic_name": "Atenolol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}], "application_number": "ANDA078512", "marketing_category": "ANDA", "marketing_start_date": "20210303", "listing_expiration_date": "20271231"}