gentamicin sulfate
Generic: gentamicin sulfate
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
gentamicin sulfate
Generic Name
gentamicin sulfate
Labeler
preferred pharmaceuticals inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
gentamicin sulfate 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7336
Product ID
68788-7336_15322965-5759-49e8-95ae-943cbdf2527e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062196
Listing Expiration
2026-12-31
Marketing Start
2019-03-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887336
Hyphenated Format
68788-7336
Supplemental Identifiers
RxCUI
UNII
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 sulfate (source: ndc)
Generic Name
gentamicin sulfate (source: ndc)
Application Number
ANDA062196 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 5 mL in 1 BOTTLE, PLASTIC (68788-7336-5)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "15322965-5759-49e8-95ae-943cbdf2527e", "openfda": {"unii": ["8X7386QRLV"], "rxcui": ["310467"], "spl_set_id": ["f91d8769-81b0-4907-b908-202f22289a89"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOTTLE, PLASTIC (68788-7336-5)", "package_ndc": "68788-7336-5", "marketing_start_date": "20190312"}], "brand_name": "Gentamicin Sulfate", "product_id": "68788-7336_15322965-5759-49e8-95ae-943cbdf2527e", "dosage_form": "SOLUTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "68788-7336", "generic_name": "Gentamicin Sulfate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gentamicin Sulfate", "active_ingredients": [{"name": "GENTAMICIN SULFATE", "strength": "3 mg/mL"}], "application_number": "ANDA062196", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}