Package 0338-9657-75

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0338-9657-75
Digits Only 0338965775
Product NDC 0338-9657
Description

50 mL in 1 BAG (0338-9657-75)

Marketing

Marketing Status
Marketed Since 2024-08-09
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ba9e58a5-60c5-4aab-9cef-36320d052091", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807632", "1807633", "1807634", "1807639"], "spl_set_id": ["958d35f0-6834-43be-a700-fa58f38b4c19"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BAG (0338-9657-75)", "package_ndc": "0338-9657-75", "marketing_start_date": "20240809"}], "brand_name": "SODIUM CHLORIDE", "product_id": "0338-9657_ba9e58a5-60c5-4aab-9cef-36320d052091", "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": "0338-9657", "generic_name": "sodium chloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 g/1000mL"}], "application_number": "NDA016677", "marketing_category": "NDA", "marketing_start_date": "19701209", "listing_expiration_date": "20271231"}