glucose

Generic: dextrose anhydrous

Labeler: baxter healthcare company
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE Inactive Finished

Drug Facts

Product Profile

Brand Name glucose
Generic Name dextrose anhydrous
Labeler baxter healthcare company
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 55 g/100mL

Manufacturer
Baxter Healthcare Company

Identifiers & Regulatory

Product NDC 0338-9787
Product ID 0338-9787_9c66f204-076e-4b1f-ad14-2b342b2ea5d5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Listing Expiration 2026-12-31
Marketing Start 2024-10-18

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03389787
Hyphenated Format 0338-9787

Supplemental Identifiers

RxCUI
2698763 2698764
UNII
LX22YL083G

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 glucose (source: ndc)
Generic Name dextrose anhydrous (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 55 g/100mL
source: ndc
Packaging
  • 4 BAG in 1 CARTON (0338-9787-04) / 3000 mL in 1 BAG (0338-9787-01)
source: ndc

Packages (1)

Ingredients (1)

dextrose monohydrate (55 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9c66f204-076e-4b1f-ad14-2b342b2ea5d5", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["2698763", "2698764"], "spl_set_id": ["5b44c747-ee6f-484a-9d42-aa04b76a5588"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BAG in 1 CARTON (0338-9787-04)  / 3000 mL in 1 BAG (0338-9787-01)", "package_ndc": "0338-9787-04", "marketing_start_date": "20241018"}], "brand_name": "Glucose", "product_id": "0338-9787_9c66f204-076e-4b1f-ad14-2b342b2ea5d5", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0338-9787", "generic_name": "Dextrose anhydrous", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glucose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "55 g/100mL"}], "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE", "marketing_start_date": "20241018", "listing_expiration_date": "20261231"}