Package 0093-2274-34

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 0093-2274-34
Digits Only 0093227434
Product NDC 0093-2274
Description

20 TABLET, FILM COATED in 1 BOTTLE (0093-2274-34)

Marketing

Marketing Status
Marketed Since 2002-10-31
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": "aaf9ce2f-41c3-489c-b5c1-f4f553d84854", "openfda": {"upc": ["0300932274341", "0300932275348"], "unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562508", "617296", "617423", "617430"], "spl_set_id": ["963e7bea-ff5d-420a-9cb2-e4aefb534b33"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (0093-2274-34)", "package_ndc": "0093-2274-34", "marketing_start_date": "20021031"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "0093-2274_aaf9ce2f-41c3-489c-b5c1-f4f553d84854", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "0093-2274", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "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": "ANDA065101", "marketing_category": "ANDA", "marketing_start_date": "20021031", "listing_expiration_date": "20261231"}