Package 63323-010-96

Brand: gentamicin

Generic: gentamicin sulfate
NDC Package

Package Facts

Identity

Package NDC 63323-010-96
Digits Only 6332301096
Product NDC 63323-010
Product ID 63323-010_092ee018-3026-4c10-a751-2043e980b09f
Description

25 VIAL, MULTI-DOSE in 1 TRAY (63323-010-96) / 20 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2000-08-10
Brand gentamicin
Generic gentamicin sulfate
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": "092ee018-3026-4c10-a751-2043e980b09f", "openfda": {"unii": ["8X7386QRLV"], "rxcui": ["313996"], "spl_set_id": ["84f5c763-1cd3-4d85-9afb-934db8666fbf"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (63323-010-96)  / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "63323-010-96", "marketing_start_date": "20000810"}], "brand_name": "Gentamicin", "product_id": "63323-010_092ee018-3026-4c10-a751-2043e980b09f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "63323-010", "generic_name": "GENTAMICIN SULFATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gentamicin", "active_ingredients": [{"name": "GENTAMICIN SULFATE", "strength": "40 mg/mL"}], "application_number": "ANDA062366", "marketing_category": "ANDA", "marketing_start_date": "20000810", "listing_expiration_date": "20261231"}