Package 0338-9151-30
Brand: sodium chloride
Generic: sodium chloridePackage Facts
Identity
Package NDC
0338-9151-30
Digits Only
0338915130
Product NDC
0338-9151
Description
50 mL in 1 BAG (0338-9151-30)
Marketing
Marketing Status
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": "39f15dfb-4e73-4959-ad9b-4ee502278b4b", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807632"], "spl_set_id": ["aeaed9cb-b629-4019-88d2-a916179427de"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BAG (0338-9151-30)", "package_ndc": "0338-9151-30", "marketing_start_date": "20210219"}], "brand_name": "SODIUM CHLORIDE", "product_id": "0338-9151_39f15dfb-4e73-4959-ad9b-4ee502278b4b", "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": "0338-9151", "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": "450 mg/50mL"}], "application_number": "NDA020178", "marketing_category": "NDA", "marketing_start_date": "19921207", "listing_expiration_date": "20261231"}