Package 16714-295-01

Brand: amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium
NDC Package

Package Facts

Identity

Package NDC 16714-295-01
Digits Only 1671429501
Product NDC 16714-295
Product ID 16714-295_ef0e5a65-a3fc-41b2-8e60-f8d056c972dd
Description

30 TABLET, FILM COATED in 1 BOTTLE (16714-295-01)

Marketing

Marketing Status
Marketed Since 2012-01-20
Brand amoxicillin and clavulanate potassium
Generic amoxicillin and clavulanate potassium
Sample Package No

Linked Drug Pages (1)

Amoxicillin and Clavulanate Potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ef0e5a65-a3fc-41b2-8e60-f8d056c972dd", "openfda": {"unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562251", "562508", "617296"], "spl_set_id": ["d75b0a7e-cb9b-4102-bcac-097403b25129"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-295-01)", "package_ndc": "16714-295-01", "marketing_start_date": "20120120"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "16714-295_ef0e5a65-a3fc-41b2-8e60-f8d056c972dd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "16714-295", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA091569", "marketing_category": "ANDA", "marketing_start_date": "20120120", "listing_expiration_date": "20261231"}