sodium chloride
Generic: sodium chloride
Labeler: b. braun medical inc.Drug Facts
Product Profile
Brand Name
sodium chloride
Generic Name
sodium chloride
Labeler
b. braun medical inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium chloride .9 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0264-7800
Product ID
0264-7800_318417ff-d599-47b8-8181-89c3bb3b2e8d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019635
Listing Expiration
2026-12-31
Marketing Start
2013-12-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02647800
Hyphenated Format
0264-7800
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
NDA019635 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .9 g/100mL
Packaging
- 12 CONTAINER in 1 CASE (0264-7800-09) / 1000 mL in 1 CONTAINER
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "318417ff-d599-47b8-8181-89c3bb3b2e8d", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807639"], "spl_set_id": ["47a0313f-36df-4fa6-a828-c9e1946ba9b0"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CONTAINER in 1 CASE (0264-7800-09) / 1000 mL in 1 CONTAINER", "package_ndc": "0264-7800-09", "marketing_start_date": "20131231"}], "brand_name": "Sodium Chloride", "product_id": "0264-7800_318417ff-d599-47b8-8181-89c3bb3b2e8d", "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": "0264-7800", "generic_name": "Sodium Chloride", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "application_number": "NDA019635", "marketing_category": "NDA", "marketing_start_date": "20131231", "listing_expiration_date": "20261231"}