Package 76420-005-20

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 76420-005-20
Digits Only 7642000520
Product NDC 76420-005
Description

20 TABLET, FILM COATED in 1 BOTTLE (76420-005-20)

Marketing

Marketing Status
Marketed Since 2020-09-01
Brand amoxicillin and clavulanate potassium
Generic amoxicillin and clavulanate potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ae61a16a-506a-9c59-e053-2995a90a4704", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["bf29327f-4e43-4597-83d2-f64349bf9d9a"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (76420-005-20)", "package_ndc": "76420-005-20", "marketing_start_date": "20200901"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "76420-005_ae61a16a-506a-9c59-e053-2995a90a4704", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "76420-005", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA204755", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}