Package 42708-012-30

Brand: atenolol

Generic: atenolol
NDC Package Sample

Package Facts

Identity

Package NDC 42708-012-30
Digits Only 4270801230
Product NDC 42708-012
Description

30 TABLET in 1 BOTTLE (42708-012-30)

Marketing

Marketing Status
Marketed Since 2018-03-14
Brand atenolol
Generic atenolol
Sample Package Yes

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b43876-f7b3-e3e8-e063-6394a90ad40a", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["70d7a585-7a46-4eac-b2b5-2ac5b98d9882"], "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 (42708-012-30)", "package_ndc": "42708-012-30", "marketing_start_date": "20180314"}], "brand_name": "Atenolol", "product_id": "42708-012_45b43876-f7b3-e3e8-e063-6394a90ad40a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42708-012", "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": "ANDA074056", "marketing_category": "ANDA", "marketing_start_date": "19950222", "listing_expiration_date": "20261231"}