Package 84549-049-48

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 84549-049-48
Digits Only 8454904948
Product NDC 84549-049
Product ID 84549-049_463e84b2-a9e7-fde6-e063-6294a90ab983
Description

100 mL in 1 BAG (84549-049-48)

Marketing

Marketing Status
Marketed Since 2025-09-23
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": "463e84b2-a9e7-fde6-e063-6294a90ab983", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807632"], "spl_set_id": ["3f79fb8b-d0e8-db2a-e063-6394a90ac136"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BAG (84549-049-48)", "package_ndc": "84549-049-48", "marketing_start_date": "20250923"}], "brand_name": "Sodium Chloride", "product_id": "84549-049_463e84b2-a9e7-fde6-e063-6294a90ab983", "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": "84549-049", "generic_name": "Sodium Chloride", "labeler_name": "ProPharma Distribution", "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": "20261231"}