dextrose and sodium chloride (0338-0077)

Drug Facts

Product Profile

Brand Name dextrose and sodium chloride

Generic Name dextrose and sodium chloride

Labeler baxter healthcare company

Dosage Form INJECTION, SOLUTION

Routes

INTRAVENOUS

Active Ingredients

dextrose monohydrate 5 g/100mL, sodium chloride 200 mg/100mL

Manufacturer

Baxter Healthcare Company

Identifiers & Regulatory

Product NDC 0338-0077

Product ID 0338-0077_b4404498-6ab7-4c25-a5a2-5377a6dfecca

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category NDA

Application Number NDA016689

Listing Expiration 2026-12-31

Marketing Start 1970-12-08

Pharmacologic Class

Classes

increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03380077

Hyphenated Format 0338-0077

Supplemental Identifiers

RxCUI

1794881 1794886 1794887 1795250 1795252 1795344 1795346 1795470

UNII

451W47IQ8X 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 dextrose and sodium chloride (source: ndc)

Generic Name dextrose and sodium chloride (source: ndc)

Application Number NDA016689 (source: ndc)

Routes

INTRAVENOUS

source: ndc

Resolved Composition

Strengths

5 g/100mL
200 mg/100mL

source: ndc

Packaging

36 BAG in 1 CARTON (0338-0077-02) / 250 mL in 1 BAG
14 BAG in 1 CARTON (0338-0077-04) / 1000 mL in 1 BAG

source: ndc

Packages (2)

0338-0077-02 36 BAG in 1 CARTON (0338-0077-02) / 250 mL in 1 BAG 0338-0077-04 14 BAG in 1 CARTON (0338-0077-04) / 1000 mL in 1 BAG

Ingredients (2)

dextrose monohydrate (5 g/100mL) sodium chloride (200 mg/100mL)

Linked Drug Pages (1)

Dextrose and Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAVENOUS"], "spl_id": "b4404498-6ab7-4c25-a5a2-5377a6dfecca", "openfda": {"unii": ["451W47IQ8X", "LX22YL083G"], "rxcui": ["1794881", "1794886", "1794887", "1795250", "1795252", "1795344", "1795346", "1795470"], "spl_set_id": ["dcbf1907-1841-4afc-ab5d-a9893a2d7256"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "36 BAG in 1 CARTON (0338-0077-02)  / 250 mL in 1 BAG", "package_ndc": "0338-0077-02", "marketing_start_date": "19701208"}, {"sample": false, "description": "14 BAG in 1 CARTON (0338-0077-04)  / 1000 mL in 1 BAG", "package_ndc": "0338-0077-04", "marketing_start_date": "19701208"}], "brand_name": "Dextrose and Sodium Chloride", "product_id": "0338-0077_b4404498-6ab7-4c25-a5a2-5377a6dfecca", "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": "0338-0077", "generic_name": "Dextrose and Sodium Chloride", "labeler_name": "Baxter Healthcare Company", "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": "200 mg/100mL"}], "application_number": "NDA016689", "marketing_category": "NDA", "marketing_start_date": "19701208", "listing_expiration_date": "20261231"}