Package 0990-8138-10

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0990-8138-10
Digits Only 0990813810
Product NDC 0990-8138
Description

12 BOTTLE, PLASTIC in 1 CASE (0990-8138-10) / 1000 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-04-01
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["IRRIGATION"], "spl_id": "74e0a747-3512-43de-a32d-64aaf439092b", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["486515"], "spl_set_id": ["97726039-847e-416f-a19a-b4060369cdad"], "manufacturer_name": ["ICU Medical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BOTTLE, PLASTIC in 1 CASE (0990-8138-10)  / 1000 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0990-8138-10", "marketing_end_date": "20260401", "marketing_start_date": "20240801"}], "brand_name": "Sodium Chloride", "product_id": "0990-8138_74e0a747-3512-43de-a32d-64aaf439092b", "dosage_form": "IRRIGANT", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0990-8138", "generic_name": "SODIUM CHLORIDE", "labeler_name": "ICU Medical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE", "marketing_end_date": "20260401", "marketing_start_date": "20240801"}