nupro chlorhexidine gluconate
Generic: chlorhexidine gluconate
Labeler: xttrium laboratories, inc.Drug Facts
Product Profile
Brand Name
nupro chlorhexidine gluconate
Generic Name
chlorhexidine gluconate
Labeler
xttrium laboratories, inc.
Dosage Form
RINSE
Routes
Active Ingredients
chlorhexidine gluconate 1.2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0116-0800
Product ID
0116-0800_34009d15-bb1b-9b7e-e063-6294a90ae5e3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077789
Listing Expiration
2026-12-31
Marketing Start
2017-01-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01160800
Hyphenated Format
0116-0800
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
nupro chlorhexidine gluconate (source: ndc)
Generic Name
chlorhexidine gluconate (source: ndc)
Application Number
ANDA077789 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.2 mg/mL
Packaging
- 473 mL in 1 BOTTLE (0116-0800-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34009d15-bb1b-9b7e-e063-6294a90ae5e3", "openfda": {"unii": ["MOR84MUD8E"], "rxcui": ["834127", "1869723"], "spl_set_id": ["4a3b87bc-d913-6c88-e054-00144ff8d46c"], "manufacturer_name": ["Xttrium Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0116-0800-16)", "package_ndc": "0116-0800-16", "marketing_start_date": "20170117"}], "brand_name": "NUPRO Chlorhexidine Gluconate", "product_id": "0116-0800_34009d15-bb1b-9b7e-e063-6294a90ae5e3", "dosage_form": "RINSE", "pharm_class": ["Decreased Cell Wall Integrity [PE]"], "product_ndc": "0116-0800", "generic_name": "CHLORHEXIDINE GLUCONATE", "labeler_name": "Xttrium Laboratories, Inc.", "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"}