sodium chloride

Generic: sodium chloride

Labeler: propharma distribution
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler propharma distribution
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 9 g/1000mL

Manufacturer
ProPharma Distribution

Identifiers & Regulatory

Product NDC 84549-049
Product ID 84549-049_463e84b2-a9e7-fde6-e063-6294a90ab983
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016677
Listing Expiration 2026-12-31
Marketing Start 1970-12-09

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84549049
Hyphenated Format 84549-049

Supplemental Identifiers

RxCUI
1807632
UNII
451W47IQ8X

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sodium chloride (source: ndc)
Generic Name sodium chloride (source: ndc)
Application Number NDA016677 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 9 g/1000mL
source: ndc
Packaging
  • 100 mL in 1 BAG (84549-049-48)
source: ndc

Packages (1)

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

Ingredients (1)

sodium chloride (9 g/1000mL)

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.9)

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"}