dextrose
Generic: dextrose monohydrate
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
dextrose
Generic Name
dextrose monohydrate
Labeler
baxter healthcare corporation
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dextrose monohydrate 2.5 g/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
0338-9651
Product ID
0338-9651_66eb82f8-6755-42aa-b20c-192a640e8068
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA016673
Listing Expiration
2026-12-31
Marketing Start
1971-03-04
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03389651
Hyphenated Format
0338-9651
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
dextrose (source: ndc)
Generic Name
dextrose monohydrate (source: ndc)
Application Number
NDA016673 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 g/50mL
Packaging
- 75 BAG in 1 CARTON (0338-9651-75) / 50 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "66eb82f8-6755-42aa-b20c-192a640e8068", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["1795607", "1795609", "1795610", "1795612", "1795616"], "spl_set_id": ["36e9478c-5df0-4b47-b97d-de3626d7cb29"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 BAG in 1 CARTON (0338-9651-75) / 50 mL in 1 BAG", "package_ndc": "0338-9651-75", "marketing_start_date": "20240809"}], "brand_name": "DEXTROSE", "product_id": "0338-9651_66eb82f8-6755-42aa-b20c-192a640e8068", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0338-9651", "generic_name": "dextrose monohydrate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROSE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "2.5 g/50mL"}], "application_number": "NDA016673", "marketing_category": "NDA", "marketing_start_date": "19710304", "listing_expiration_date": "20261231"}