Package 0990-7983-61

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0990-7983-61
Digits Only 0990798361
Product NDC 0990-7983
Description

32 POUCH in 1 CASE (0990-7983-61) / 1 BAG in 1 POUCH / 150 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2019-11-01
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "beda0179-f554-4c42-b60e-68615243d312", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807548", "1807549", "1807550", "1807551", "1807552", "1807627", "1807630", "1807631", "1807632", "1807633", "1807634", "1807639"], "spl_set_id": ["5f372b75-d7a4-471e-8ac6-290040fc84b0"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (0990-7983-02)  / 1 BAG in 1 POUCH / 250 mL in 1 BAG", "package_ndc": "0990-7983-02", "marketing_start_date": "20190501"}, {"sample": false, "description": "24 POUCH in 1 CASE (0990-7983-03)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG", "package_ndc": "0990-7983-03", "marketing_start_date": "20191231"}, {"sample": false, "description": "12 POUCH in 1 CASE (0990-7983-09)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-7983-09", "marketing_start_date": "20191115"}, {"sample": false, "description": "24 POUCH in 1 CASE (0990-7983-53)  / 1 BAG in 1 POUCH / 250 mL in 1 BAG", "package_ndc": "0990-7983-53", "marketing_start_date": "20191231"}, {"sample": false, "description": "18 POUCH in 1 CASE (0990-7983-55)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG", "package_ndc": "0990-7983-55", "marketing_start_date": "20191231"}, {"sample": false, "description": "32 POUCH in 1 CASE (0990-7983-61)  / 1 BAG in 1 POUCH / 150 mL in 1 BAG", "package_ndc": "0990-7983-61", "marketing_start_date": "20191101"}], "brand_name": "Sodium Chloride", "product_id": "0990-7983_beda0179-f554-4c42-b60e-68615243d312", "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": "0990-7983", "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"}], "application_number": "NDA016366", "marketing_category": "NDA", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}