Package 67296-1921-7

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 67296-1921-7
Digits Only 6729619217
Product NDC 67296-1921
Description

75 mL in 1 BOTTLE (67296-1921-7)

Marketing

Marketing Status
Marketed Since 2022-09-19
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": "4727cd5c-c786-7e6f-e063-6294a90a57ea", "openfda": {"upc": ["0381964203691", "0381964203547"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["2fbb57ba-08d8-0224-e063-6294a90ab683"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (67296-1921-7)", "package_ndc": "67296-1921-7", "marketing_start_date": "20220919"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "67296-1921_4727cd5c-c786-7e6f-e063-6294a90a57ea", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "67296-1921", "generic_name": "amoxicillin and clavulanate potassium", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "NDA050755", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220919", "listing_expiration_date": "20261231"}