Package 0338-9799-12

Brand: glucose and sodium chloride

Generic: dextrose anhydrous and sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0338-9799-12
Digits Only 0338979912
Product NDC 0338-9799
Product ID 0338-9799_bf7a8e49-ae3a-484a-8437-d8dd72faba49
Description

12 BAG in 1 CARTON (0338-9799-12) / 1000 mL in 1 BAG (0338-9799-01)

Marketing

Marketing Status
Marketed Since 2024-10-11
Brand glucose and sodium chloride
Generic dextrose anhydrous and sodium chloride
Sample Package No

Linked Drug Pages (1)

Glucose and Sodium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "bf7a8e49-ae3a-484a-8437-d8dd72faba49", "openfda": {"unii": ["LX22YL083G", "451W47IQ8X"], "rxcui": ["2698222"], "spl_set_id": ["1ba918d0-13d0-48bc-8742-658fc0eb47b6"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BAG in 1 CARTON (0338-9799-12)  / 1000 mL in 1 BAG (0338-9799-01)", "package_ndc": "0338-9799-12", "marketing_start_date": "20241011"}], "brand_name": "Glucose and Sodium Chloride", "product_id": "0338-9799_bf7a8e49-ae3a-484a-8437-d8dd72faba49", "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": "0338-9799", "generic_name": "Dextrose Anhydrous and Sodium Chloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glucose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5.5 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE", "marketing_start_date": "20241011", "listing_expiration_date": "20261231"}