Package 0143-9129-10

Brand: gentamicin

Generic: gentamicin
NDC Package

Package Facts

Identity

Package NDC 0143-9129-10
Digits Only 0143912910
Product NDC 0143-9129
Product ID 0143-9129_9908273d-c700-4036-82fe-312f25a8aacd
Description

10 VIAL in 1 CARTON (0143-9129-10) / 20 mL in 1 VIAL (0143-9129-01)

Marketing

Marketing Status
Marketed Since 2022-02-15
Brand gentamicin
Generic gentamicin
Sample Package No

Linked Drug Pages (1)

Gentamicin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "9908273d-c700-4036-82fe-312f25a8aacd", "openfda": {"unii": ["8X7386QRLV"], "rxcui": ["313996"], "spl_set_id": ["51fffac8-fb6e-4f7f-b2de-440252781a42"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9129-10)  / 20 mL in 1 VIAL (0143-9129-01)", "package_ndc": "0143-9129-10", "marketing_start_date": "20220215"}], "brand_name": "Gentamicin", "product_id": "0143-9129_9908273d-c700-4036-82fe-312f25a8aacd", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "0143-9129", "generic_name": "Gentamicin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gentamicin", "active_ingredients": [{"name": "GENTAMICIN SULFATE", "strength": "40 mg/mL"}], "application_number": "ANDA062251", "marketing_category": "ANDA", "marketing_start_date": "20220215", "listing_expiration_date": "20261231"}