Package 72189-385-32

Brand: amoxil

Generic: amoxicillin oral susp
NDC Package

Package Facts

Identity

Package NDC 72189-385-32
Digits Only 7218938532
Product NDC 72189-385
Product ID 72189-385_2c4cbe6c-c27d-15fe-e063-6294a90ac409
Description

100 mL in 1 BOTTLE (72189-385-32)

Marketing

Marketing Status
Marketed Since 2022-10-21
Brand amoxil
Generic amoxicillin oral susp
Sample Package No

Linked Drug Pages (1)

Amoxil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4cbe6c-c27d-15fe-e063-6294a90ac409", "openfda": {"unii": ["804826J2HU"], "spl_set_id": ["ec7dd735-dc92-3d29-e053-2a95a90af549"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (72189-385-32)", "package_ndc": "72189-385-32", "marketing_start_date": "20221021"}], "brand_name": "Amoxil", "product_id": "72189-385_2c4cbe6c-c27d-15fe-e063-6294a90ac409", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "72189-385", "generic_name": "Amoxicillin Oral Susp", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxil", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "400 mg/5mL"}], "application_number": "ANDA065325", "marketing_category": "ANDA", "marketing_start_date": "20221021", "listing_expiration_date": "20261231"}