Package 63187-320-00

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 63187-320-00
Digits Only 6318732000
Product NDC 63187-320
Description

100 mL in 1 BOTTLE (63187-320-00)

Marketing

Marketing Status
Marketed Since 2015-02-02
Brand amoxicillin and clavulanate potassium
Generic amoxicillin and clavulanate potassium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8c98b649-b901-4213-9713-757845f5997a", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617430"], "spl_set_id": ["1f252ad3-373c-4a6d-96e7-53ba820d201b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (63187-320-00)", "package_ndc": "63187-320-00", "marketing_start_date": "20150202"}], "brand_name": "amoxicillin and clavulanate potassium", "product_id": "63187-320_8c98b649-b901-4213-9713-757845f5997a", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "63187-320", "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": "400 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "57 mg/5mL"}], "application_number": "NDA050725", "marketing_category": "NDA", "marketing_start_date": "19901022", "listing_expiration_date": "20261231"}