Package 71205-035-30

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 71205-035-30
Digits Only 7120503530
Product NDC 71205-035
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-035-30)

Marketing

Marketing Status
Marketed Since 2018-05-01
Brand amoxicillin
Generic amoxicillin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "23c32fbb-0d4d-4830-883f-0967c8586247", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["7974a666-6d1d-446b-8ea5-f7145dc66358"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71205-035-14)", "package_ndc": "71205-035-14", "marketing_start_date": "20190901"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-035-20)", "package_ndc": "71205-035-20", "marketing_start_date": "20180501"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-035-30)", "package_ndc": "71205-035-30", "marketing_start_date": "20180501"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-035-60)", "package_ndc": "71205-035-60", "marketing_start_date": "20180501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-035-90)", "package_ndc": "71205-035-90", "marketing_start_date": "20180501"}], "brand_name": "Amoxicillin", "product_id": "71205-035_23c32fbb-0d4d-4830-883f-0967c8586247", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "71205-035", "generic_name": "Amoxicillin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065228", "marketing_category": "ANDA", "marketing_start_date": "20050713", "listing_expiration_date": "20261231"}