Package 42708-162-30

Brand: atenolol

Generic: atenolol
NDC Package Sample

Package Facts

Identity

Package NDC 42708-162-30
Digits Only 4270816230
Product NDC 42708-162
Description

30 TABLET in 1 BOTTLE, PLASTIC (42708-162-30)

Marketing

Marketing Status
Marketed Since 2023-03-13
Brand atenolol
Generic atenolol
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459bcfe8-f4d3-8c23-e063-6394a90a26de", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["f682a775-2255-05e2-e053-2a95a90ac3f3"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE, PLASTIC (42708-162-30)", "package_ndc": "42708-162-30", "marketing_start_date": "20230313"}], "brand_name": "Atenolol", "product_id": "42708-162_459bcfe8-f4d3-8c23-e063-6394a90a26de", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42708-162", "generic_name": "Atenolol", "labeler_name": "QPharma 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": "20071031", "listing_expiration_date": "20261231"}