Package 72189-359-05

Brand: gentamicin sulfate opth solution

Generic: gentamicin sulfate opth solution
NDC Package

Package Facts

Identity

Package NDC 72189-359-05
Digits Only 7218935905
Product NDC 72189-359
Description

5 mL in 1 BOTTLE, DROPPER (72189-359-05)

Marketing

Marketing Status
Marketed Since 2022-06-17
Brand gentamicin sulfate opth solution
Generic gentamicin sulfate opth solution
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "2c4c8caf-089b-acf6-e063-6294a90a14c3", "openfda": {"unii": ["8X7386QRLV"], "rxcui": ["310467"], "spl_set_id": ["e1a5bc32-f9a0-6b33-e053-2995a90ab9ac"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 BOTTLE, DROPPER (72189-359-05)", "package_ndc": "72189-359-05", "marketing_start_date": "20220617"}], "brand_name": "Gentamicin Sulfate Opth Solution", "product_id": "72189-359_2c4c8caf-089b-acf6-e063-6294a90a14c3", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "72189-359", "generic_name": "Gentamicin Sulfate Opth Solution", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gentamicin Sulfate Opth Solution", "active_ingredients": [{"name": "GENTAMICIN SULFATE", "strength": "3 mg/mL"}], "application_number": "ANDA064048", "marketing_category": "ANDA", "marketing_start_date": "20220617", "listing_expiration_date": "20261231"}