Package 63323-095-61

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 63323-095-61
Digits Only 6332309561
Product NDC 63323-095
Product ID 63323-095_5db02ff9-4936-46b0-8fb5-3fc491895ae1
Description

20 VIAL, PLASTIC in 1 TRAY (63323-095-61) / 100 mL in 1 VIAL, PLASTIC (63323-095-02)

Marketing

Marketing Status
Marketed Since 2022-02-14
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "5db02ff9-4936-46b0-8fb5-3fc491895ae1", "openfda": {"upc": ["0363323095024"], "unii": ["451W47IQ8X"], "rxcui": ["313016"], "spl_set_id": ["8b44bfd3-70a4-4b47-bc7b-590f63b8cc75"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL, PLASTIC in 1 TRAY (63323-095-61)  / 100 mL in 1 VIAL, PLASTIC (63323-095-02)", "package_ndc": "63323-095-61", "marketing_start_date": "20220214"}], "brand_name": "Sodium Chloride", "product_id": "63323-095_5db02ff9-4936-46b0-8fb5-3fc491895ae1", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "63323-095", "generic_name": "Sodium Chloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "4 meq/mL"}], "application_number": "ANDA212070", "marketing_category": "ANDA", "marketing_start_date": "20220214", "listing_expiration_date": "20261231"}