sodium chloride

Generic: sodium chloride

Labeler: icu medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler icu medical inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 450 mg/100mL

Manufacturer
ICU Medical Inc.

Identifiers & Regulatory

Product NDC 0990-7730
Product ID 0990-7730_beda0179-f554-4c42-b60e-68615243d312
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018090
Listing Expiration 2026-12-31
Marketing Start 2019-04-01

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 09907730
Hyphenated Format 0990-7730

Supplemental Identifiers

RxCUI
1807548 1807549 1807550 1807551 1807552 1807627 1807630 1807631 1807632 1807633 1807634 1807639
UNII
451W47IQ8X

Packaging Origin

Original Packager
true

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 NDA018090 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 450 mg/100mL
source: ndc
Packaging
  • 20 POUCH in 1 CASE (0990-7730-36) / 4 BAG in 1 POUCH / 50 mL in 1 BAG
  • 20 POUCH in 1 CASE (0990-7730-37) / 4 BAG in 1 POUCH / 100 mL in 1 BAG
source: ndc

Packages (2)

0990-7730-36 20 POUCH in 1 CASE (0990-7730-36) / 4 BAG in 1 POUCH / 50 mL in 1 BAG 0990-7730-37 20 POUCH in 1 CASE (0990-7730-37) / 4 BAG in 1 POUCH / 100 mL in 1 BAG

Ingredients (1)

sodium chloride (450 mg/100mL)

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.9)

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": "20 POUCH in 1 CASE (0990-7730-36)  / 4 BAG in 1 POUCH / 50 mL in 1 BAG", "package_ndc": "0990-7730-36", "marketing_start_date": "20191231"}, {"sample": false, "description": "20 POUCH in 1 CASE (0990-7730-37)  / 4 BAG in 1 POUCH / 100 mL in 1 BAG", "package_ndc": "0990-7730-37", "marketing_start_date": "20191231"}], "brand_name": "Sodium Chloride", "product_id": "0990-7730_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": "0990-7730", "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": "450 mg/100mL"}], "application_number": "NDA018090", "marketing_category": "NDA", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}