Package 68788-8836-2

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 68788-8836-2
Digits Only 6878888362
Product NDC 68788-8836
Description

20 TABLET, FILM COATED in 1 BOTTLE (68788-8836-2)

Marketing

Marketing Status
Marketed Since 2025-02-27
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": "a0822381-ba9a-4f80-bc4f-608301d07fd8", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["a0822381-ba9a-4f80-bc4f-608301d07fd8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8836-2)", "package_ndc": "68788-8836-2", "marketing_start_date": "20250227"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68788-8836_a0822381-ba9a-4f80-bc4f-608301d07fd8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68788-8836", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Preferred Pharmaceuticals 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": "ANDA091568", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}