Package 60758-188-05
Brand: GENTAMICIN SULFATE
Generic: gentamicin sulfatePackage Facts
Identity
Package NDC
60758-188-05
Digits Only
6075818805
Product NDC
60758-188
Description
1 BOTTLE, DROPPER in 1 CARTON (60758-188-05) / 5 mL in 1 BOTTLE, DROPPER
Marketing
Marketing Status
Brand
GENTAMICIN SULFATE
Generic
gentamicin sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "0b295ef8-52d7-4199-91f4-53838936257a", "openfda": {"unii": ["8X7386QRLV"], "rxcui": ["310467"], "spl_set_id": ["0bc9fa00-1755-4989-a222-a038e970371f"], "manufacturer_name": ["Pacific Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (60758-188-05) / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "60758-188-05", "marketing_start_date": "19980105"}], "brand_name": "GENTAMICIN SULFATE", "product_id": "60758-188_0b295ef8-52d7-4199-91f4-53838936257a", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "60758-188", "generic_name": "gentamicin sulfate", "labeler_name": "Pacific Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GENTAMICIN SULFATE", "active_ingredients": [{"name": "GENTAMICIN SULFATE", "strength": "3 mg/mL"}], "application_number": "ANDA062452", "marketing_category": "ANDA", "marketing_start_date": "19980105", "listing_expiration_date": "20261231"}