Package 60758-188-05

Brand: GENTAMICIN SULFATE

Generic: gentamicin sulfate
NDC Package

Package 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
Marketed Since 1998-01-05
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"}