sodium chloride

Generic: sodium chloride

Labeler: medefil, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler medefil, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

sodium chloride 9 mg/mL

Manufacturer
Medefil, Inc.

Identifiers & Regulatory

Product NDC 64253-202
Product ID 64253-202_4bbe9ad8-075c-216b-e063-6294a90a1024
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA202832
Listing Expiration 2027-12-31
Marketing Start 2012-01-13

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 64253202
Hyphenated Format 64253-202

Supplemental Identifiers

RxCUI
727820
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 NDA202832 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 60 SYRINGE, PLASTIC in 1 BOX (64253-202-30) / 10 mL in 1 SYRINGE, PLASTIC
source: ndc

Packages (1)

64253-202-30 60 SYRINGE, PLASTIC in 1 BOX (64253-202-30) / 10 mL in 1 SYRINGE, PLASTIC

Ingredients (1)

sodium chloride (9 mg/mL)

Linked Drug Pages (1)

sodium chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "4bbe9ad8-075c-216b-e063-6294a90a1024", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["727820"], "spl_set_id": ["d1468c0f-dd4f-4d38-a84c-c1d110303965"], "manufacturer_name": ["Medefil, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 SYRINGE, PLASTIC in 1 BOX (64253-202-30)  / 10 mL in 1 SYRINGE, PLASTIC", "package_ndc": "64253-202-30", "marketing_start_date": "20120113"}], "brand_name": "sodium chloride", "product_id": "64253-202_4bbe9ad8-075c-216b-e063-6294a90a1024", "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": "64253-202", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Medefil, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sodium chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "NDA202832", "marketing_category": "NDA", "marketing_start_date": "20120113", "listing_expiration_date": "20271231"}