Package 65222-800-16

Brand: nupro chlorhexidine gluconate

Generic: chlorhexidine gluconate
NDC Package

Package Facts

Identity

Package NDC 65222-800-16
Digits Only 6522280016
Product NDC 65222-800
Description

473 mL in 1 BOTTLE (65222-800-16)

Marketing

Marketing Status
Marketed Since 2017-01-17
Brand nupro chlorhexidine gluconate
Generic chlorhexidine gluconate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "efbafc69-96f1-451d-aa6a-26d98e0e42dc", "openfda": {"unii": ["MOR84MUD8E"], "rxcui": ["834127", "1869723"], "spl_set_id": ["d9d25abd-c3b4-4713-91c7-538f98e8fb70"], "manufacturer_name": ["Dentsply LLC. Professional Division Trading as \"DENTSPLY Professional\""], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (65222-800-16)", "package_ndc": "65222-800-16", "marketing_start_date": "20170117"}], "brand_name": "NUPRO Chlorhexidine Gluconate", "product_id": "65222-800_efbafc69-96f1-451d-aa6a-26d98e0e42dc", "dosage_form": "RINSE", "pharm_class": ["Decreased Cell Wall Integrity [PE]"], "product_ndc": "65222-800", "generic_name": "CHLORHEXIDINE GLUCONATE", "labeler_name": "Dentsply LLC. Professional Division Trading as \"DENTSPLY Professional\"", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NUPRO Chlorhexidine Gluconate", "active_ingredients": [{"name": "CHLORHEXIDINE GLUCONATE", "strength": "1.2 mg/mL"}], "application_number": "ANDA077789", "marketing_category": "ANDA", "marketing_start_date": "20170117", "listing_expiration_date": "20261231"}