Package 71335-2824-1

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 71335-2824-1
Digits Only 7133528241
Product NDC 71335-2824
Description

20 TABLET, FILM COATED in 1 BOTTLE (71335-2824-1)

Marketing

Marketing Status
Marketed Since 2025-10-23
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": "41da5422-4024-5aeb-e063-6394a90ac731", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["b5e66987-09e3-45b2-88ba-59c8647d724e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2824-1)", "package_ndc": "71335-2824-1", "marketing_start_date": "20251023"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "71335-2824_41da5422-4024-5aeb-e063-6394a90ac731", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "71335-2824", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA205707", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}