atenolol 29300-411

Generic: atenolol

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

Drug Facts

Product Profile

Brand Name atenolol 29300-411
Generic Name atenolol
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3694
Product ID 68071-3694_2a31d713-770d-8310-e063-6394a90a2406
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 680713694
Hyphenated Format 68071-3694

Supplemental Identifiers

RxCUI
197381
UPC
0368071369410
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 29300-411 (source: ndc)
Generic Name atenolol (source: ndc)
Application Number ANDA213136 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68071-3694-1)
source: ndc

Packages (1)

68071-3694-1 100 TABLET in 1 BOTTLE (68071-3694-1)

Ingredients (1)

atenolol (50 mg/1)

Linked Drug Pages (1)

Atenolol 29300-411 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a31d713-770d-8310-e063-6394a90a2406", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0368071369410"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["239b1cce-3b1a-f049-e063-6394a90a0e0a"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3694-1)", "package_ndc": "68071-3694-1", "marketing_start_date": "20241003"}], "brand_name": "Atenolol 29300-411", "product_id": "68071-3694_2a31d713-770d-8310-e063-6394a90a2406", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3694", "generic_name": "Atenolol", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "brand_name_suffix": "29300-411", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}], "application_number": "ANDA213136", "marketing_category": "ANDA", "marketing_start_date": "20191121", "listing_expiration_date": "20261231"}