Package 70882-114-20

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 70882-114-20
Digits Only 7088211420
Product NDC 70882-114
Description

20 CAPSULE in 1 BLISTER PACK (70882-114-20)

Marketing

Marketing Status
Marketed Since 1994-09-30
Brand amoxicillin
Generic amoxicillin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "af0ae6a3-1435-40dd-a62a-ce533791a28c", "openfda": {"upc": ["0370882113304", "0370882114202"], "unii": ["804826J2HU"], "rxcui": ["308182", "308191"], "spl_set_id": ["2f27307c-27a9-4ec3-bccd-d0d13d86b185"], "manufacturer_name": ["Cambridge Therapeutics Technologies, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BLISTER PACK (70882-114-20)", "package_ndc": "70882-114-20", "marketing_start_date": "19940930"}], "brand_name": "Amoxicillin", "product_id": "70882-114_af0ae6a3-1435-40dd-a62a-ce533791a28c", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70882-114", "generic_name": "Amoxicillin", "labeler_name": "Cambridge Therapeutics Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA064076", "marketing_category": "ANDA", "marketing_start_date": "19940930", "listing_expiration_date": "20261231"}