nupro chlorhexidine gluconate

Generic: chlorhexidine gluconate

Labeler: xttrium laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nupro chlorhexidine gluconate
Generic Name chlorhexidine gluconate
Labeler xttrium laboratories, inc.
Dosage Form RINSE
Routes
ORAL
Active Ingredients

chlorhexidine gluconate 1.2 mg/mL

Manufacturer
Xttrium Laboratories, Inc.

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
decreased cell wall integrity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01160800
Hyphenated Format 0116-0800

Supplemental Identifiers

RxCUI
834127 1869723
UNII
MOR84MUD8E

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.2 mg/mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (0116-0800-16)
source: ndc

Packages (1)

Ingredients (1)

chlorhexidine gluconate (1.2 mg/mL)

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"}