dextrose and sodium chloride
Generic: dextrose monohydrate and sodium chloride
Labeler: icu medical inc.Drug Facts
Product Profile
Brand Name
dextrose and sodium chloride
Generic Name
dextrose monohydrate and sodium chloride
Labeler
icu medical inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dextrose monohydrate 5 g/100mL, sodium chloride .45 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0990-7926
Product ID
0990-7926_391a9854-64db-4da4-b8a5-a230001aa81c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017607
Listing Expiration
2026-12-31
Marketing Start
2019-09-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09907926
Hyphenated Format
0990-7926
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 and sodium chloride (source: ndc)
Generic Name
dextrose monohydrate and sodium chloride (source: ndc)
Application Number
NDA017607 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 g/100mL
- .45 g/100mL
Packaging
- 24 POUCH in 1 CASE (0990-7926-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG
- 24 POUCH in 1 CASE (0990-7926-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG
- 12 POUCH in 1 CASE (0990-7926-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "391a9854-64db-4da4-b8a5-a230001aa81c", "openfda": {"unii": ["451W47IQ8X", "LX22YL083G"], "rxcui": ["1794902", "1794904", "1794905", "1795149", "1795150", "1795250", "1795252", "1795254", "1795344", "1795346"], "spl_set_id": ["4555b1bf-6d97-4798-a63d-6d34291c85ce"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (0990-7926-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG", "package_ndc": "0990-7926-02", "marketing_start_date": "20190901"}, {"sample": false, "description": "24 POUCH in 1 CASE (0990-7926-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG", "package_ndc": "0990-7926-03", "marketing_start_date": "20191201"}, {"sample": false, "description": "12 POUCH in 1 CASE (0990-7926-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-7926-09", "marketing_start_date": "20191201"}], "brand_name": "Dextrose and Sodium Chloride", "product_id": "0990-7926_391a9854-64db-4da4-b8a5-a230001aa81c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0990-7926", "generic_name": "DEXTROSE MONOHYDRATE and SODIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".45 g/100mL"}], "application_number": "NDA017607", "marketing_category": "NDA", "marketing_start_date": "20190901", "listing_expiration_date": "20261231"}