Package 0338-0162-01

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0338-0162-01
Digits Only 0338016201
Product NDC 0338-0162
Description

30 BAG in 1 CARTON (0338-0162-01) / 100 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2022-12-07
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": "61d9ec19-c2d4-44a5-935c-40c31a67b0b6", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807548", "1807631", "1807632"], "spl_set_id": ["123bd10a-90c7-499e-97f6-acf7e0f0fb4e"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BAG in 1 CARTON (0338-0162-01)  / 100 mL in 1 BAG", "package_ndc": "0338-0162-01", "marketing_start_date": "20221207"}], "brand_name": "SODIUM CHLORIDE", "product_id": "0338-0162_61d9ec19-c2d4-44a5-935c-40c31a67b0b6", "dosage_form": "INJECTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0338-0162", "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": "900 mg/100mL"}], "application_number": "NDA020178", "marketing_category": "NDA", "marketing_start_date": "19921207", "listing_expiration_date": "20261231"}