Package 63323-173-95

Brand: gentamicin

Generic: gentamicin
NDC Package

Package Facts

Identity

Package NDC 63323-173-95
Digits Only 6332317395
Product NDC 63323-173
Description

25 VIAL in 1 TRAY (63323-173-95) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2004-11-29
Brand gentamicin
Generic gentamicin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "9f48c9f7-08fd-4652-911c-c2c221a34ed3", "openfda": {"upc": ["0363323173951"], "unii": ["8X7386QRLV"], "rxcui": ["1870676"], "spl_set_id": ["63413469-c676-48a3-a945-7d2489b535ef"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (63323-173-95)  / 2 mL in 1 VIAL", "package_ndc": "63323-173-95", "marketing_start_date": "20041129"}], "brand_name": "Gentamicin", "product_id": "63323-173_9f48c9f7-08fd-4652-911c-c2c221a34ed3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "63323-173", "generic_name": "GENTAMICIN", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gentamicin", "active_ingredients": [{"name": "GENTAMICIN SULFATE", "strength": "10 mg/mL"}], "application_number": "ANDA062366", "marketing_category": "ANDA", "marketing_start_date": "20041129", "listing_expiration_date": "20261231"}