sodium chloride
Generic: sodium chloride
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
sodium chloride
Generic Name
sodium chloride
Labeler
rising pharma holdings, inc.
Dosage Form
TABLET
Routes
Active Ingredients
sodium chloride 1000 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
57237-361
Product ID
57237-361_7269ab59-c9e8-4e4f-b3c9-72d40f7abbb8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M018
Listing Expiration
2026-12-31
Marketing Start
2025-11-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
57237361
Hyphenated Format
57237-361
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
M018 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (57237-361-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7269ab59-c9e8-4e4f-b3c9-72d40f7abbb8", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["313009"], "spl_set_id": ["42870188-b1d7-4934-a6c0-310530497dac"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (57237-361-01)", "package_ndc": "57237-361-01", "marketing_start_date": "20251106"}], "brand_name": "Sodium Chloride", "product_id": "57237-361_7269ab59-c9e8-4e4f-b3c9-72d40f7abbb8", "dosage_form": "TABLET", "product_ndc": "57237-361", "generic_name": "Sodium Chloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "1000 mg/1"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251106", "listing_expiration_date": "20261231"}