Package 63187-803-20

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 63187-803-20
Digits Only 6318780320
Product NDC 63187-803
Description

20 TABLET, FILM COATED in 1 BOTTLE (63187-803-20)

Marketing

Marketing Status
Marketed Since 2017-01-02
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": "c7442c05-30ea-427d-b832-611e0d1c392f", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["01b30abb-db63-4257-9fe2-9107bb0bd69c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (63187-803-20)", "package_ndc": "63187-803-20", "marketing_start_date": "20170102"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "63187-803_c7442c05-30ea-427d-b832-611e0d1c392f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "63187-803", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Proficient Rx LP", "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": "ANDA065064", "marketing_category": "ANDA", "marketing_start_date": "20020315", "listing_expiration_date": "20261231"}