atenolol

Generic: atenolol

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol
Generic Name atenolol
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 100 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-412
Product ID 29300-412_b84110b2-cefb-49d0-8b08-1057dbdc258b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213136
Listing Expiration 2026-12-31
Marketing Start 2019-11-21

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 29300412
Hyphenated Format 29300-412

Supplemental Identifiers

RxCUI
197379 197380 197381
UNII
50VV3VW0TI
NUI
N0000000161 N0000175556

Packaging Origin

Original Packager
true

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
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (29300-412-01)
  • 500 TABLET in 1 BOTTLE (29300-412-05)
  • 1000 TABLET in 1 BOTTLE (29300-412-10)
source: ndc

Packages (3)

29300-412-01 100 TABLET in 1 BOTTLE (29300-412-01) 29300-412-05 500 TABLET in 1 BOTTLE (29300-412-05) 29300-412-10 1000 TABLET in 1 BOTTLE (29300-412-10)

Ingredients (1)

atenolol (100 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": "b84110b2-cefb-49d0-8b08-1057dbdc258b", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197379", "197380", "197381"], "spl_set_id": ["35d99c43-7305-4a4a-886e-a9bf3ee88fa8"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (29300-412-01)", "package_ndc": "29300-412-01", "marketing_start_date": "20200106"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (29300-412-05)", "package_ndc": "29300-412-05", "marketing_start_date": "20200106"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (29300-412-10)", "package_ndc": "29300-412-10", "marketing_start_date": "20220826"}], "brand_name": "Atenolol", "product_id": "29300-412_b84110b2-cefb-49d0-8b08-1057dbdc258b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "29300-412", "generic_name": "Atenolol", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "100 mg/1"}], "application_number": "ANDA213136", "marketing_category": "ANDA", "marketing_start_date": "20191121", "listing_expiration_date": "20261231"}