gentamicin
Generic: gentamicin sulfate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
gentamicin
Generic Name
gentamicin sulfate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
gentamicin sulfate 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-010
Product ID
63323-010_092ee018-3026-4c10-a751-2043e980b09f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062366
Listing Expiration
2026-12-31
Marketing Start
2000-08-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323010
Hyphenated Format
63323-010
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
gentamicin (source: ndc)
Generic Name
gentamicin sulfate (source: ndc)
Application Number
ANDA062366 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 TRAY (63323-010-96) / 20 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (3)
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"}