sodium chloride
Generic: sodium chloride tablet
Labeler: belleview bioscience llcDrug Facts
Product Profile
Brand Name
sodium chloride
Generic Name
sodium chloride tablet
Labeler
belleview bioscience llc
Dosage Form
TABLET
Routes
Active Ingredients
sodium chloride 1000 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
84447-002
Product ID
84447-002_31195e8f-d4df-9e37-e063-6294a90a4156
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M018
Listing Expiration
2026-12-31
Marketing Start
2025-03-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84447002
Hyphenated Format
84447-002
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 tablet (source: ndc)
Application Number
M018 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (84447-002-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31195e8f-d4df-9e37-e063-6294a90a4156", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["313009"], "spl_set_id": ["31195e8f-d4de-9e37-e063-6294a90a4156"], "manufacturer_name": ["Belleview Bioscience LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (84447-002-01)", "package_ndc": "84447-002-01", "marketing_start_date": "20250301"}], "brand_name": "Sodium Chloride", "product_id": "84447-002_31195e8f-d4df-9e37-e063-6294a90a4156", "dosage_form": "TABLET", "product_ndc": "84447-002", "generic_name": "Sodium Chloride Tablet", "labeler_name": "Belleview Bioscience LLC", "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": "20250301", "listing_expiration_date": "20261231"}