Package 68788-8000-1

Brand: Amoxicillin and Clavulanate Potassium

Generic: Amoxicillin and Clavulanate Potassium
NDC Package

Package Facts

Identity

Package NDC 68788-8000-1
Digits Only 6878880001
Product NDC 68788-8000
Description

100 mL in 1 BOTTLE (68788-8000-1)

Marketing

Marketing Status
Marketed Since 2021-08-10
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": "3ffb94bf-62b9-4eb0-8821-4f29ca02a094", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617423"], "spl_set_id": ["51ee76f6-b699-4e50-b7a9-0477580d1f14"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-8000-1)", "package_ndc": "68788-8000-1", "marketing_start_date": "20210810"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68788-8000_3ffb94bf-62b9-4eb0-8821-4f29ca02a094", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68788-8000", "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": "200 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "28.5 mg/5mL"}], "application_number": "ANDA065066", "marketing_category": "ANDA", "marketing_start_date": "20210810", "listing_expiration_date": "20261231"}