atenolol

Generic: atenolol

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7616
Product ID 68788-7616_8144c92d-a041-42b8-949f-b7949f91bccf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077443
Listing Expiration 2027-12-31
Marketing Start 2020-02-07

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 687887616
Hyphenated Format 68788-7616

Supplemental Identifiers

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 ANDA077443 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-7616-1)
  • 30 TABLET in 1 BOTTLE (68788-7616-3)
  • 60 TABLET in 1 BOTTLE (68788-7616-6)
  • 90 TABLET in 1 BOTTLE (68788-7616-9)
source: ndc

Packages (4)

68788-7616-1 100 TABLET in 1 BOTTLE (68788-7616-1) 68788-7616-3 30 TABLET in 1 BOTTLE (68788-7616-3) 68788-7616-6 60 TABLET in 1 BOTTLE (68788-7616-6) 68788-7616-9 90 TABLET in 1 BOTTLE (68788-7616-9)

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": "8144c92d-a041-42b8-949f-b7949f91bccf", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "spl_set_id": ["a8d48a47-ccab-4a35-a092-6e562683ade3"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7616-1)", "package_ndc": "68788-7616-1", "marketing_start_date": "20200207"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7616-3)", "package_ndc": "68788-7616-3", "marketing_start_date": "20200207"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7616-6)", "package_ndc": "68788-7616-6", "marketing_start_date": "20200207"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7616-9)", "package_ndc": "68788-7616-9", "marketing_start_date": "20200207"}], "brand_name": "Atenolol", "product_id": "68788-7616_8144c92d-a041-42b8-949f-b7949f91bccf", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-7616", "generic_name": "Atenolol", "labeler_name": "Preferred 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": "20200207", "listing_expiration_date": "20271231"}