Package 68071-4967-2

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 68071-4967-2
Digits Only 6807149672
Product NDC 68071-4967
Description

20 TABLET in 1 BOTTLE (68071-4967-2)

Marketing

Marketing Status
Marketed Since 2019-07-15
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": "4604b05b-cda3-9410-e063-6394a90ab875", "openfda": {"upc": ["0368071496727"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["8dba4e86-5f79-0bea-e053-2a95a90a9e2d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-4967-2)", "package_ndc": "68071-4967-2", "marketing_start_date": "20190715"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68071-4967_4604b05b-cda3-9410-e063-6394a90ab875", "dosage_form": "TABLET", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-4967", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "NuCare 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": "ANDA203824", "marketing_category": "ANDA", "marketing_start_date": "20160823", "listing_expiration_date": "20261231"}