sodium chloride

Generic: sodium chloride

Labeler: nephron pharmaceuticals corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler nephron pharmaceuticals corporation
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 9 mg/mL

Manufacturer
Nephron Pharmaceuticals Corporation

Identifiers & Regulatory

Product NDC 0487-4301
Product ID 0487-4301_49545dc2-5776-da02-e063-6394a90a7ef0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211968
Listing Expiration 2027-12-31
Marketing Start 2020-06-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04874301
Hyphenated Format 0487-4301

Supplemental Identifiers

RxCUI
1807631 1807632 1807633 1807634
UPC
0304874301257 0000000000000 0304874301509 0304874301059 0304874301103
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 ANDA211968 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 64 BAG in 1 CASE (0487-4301-05) / 50 mL in 1 BAG
  • 64 BAG in 1 CASE (0487-4301-10) / 100 mL in 1 BAG
  • 35 BAG in 1 CASE (0487-4301-25) / 250 mL in 1 BAG
  • 18 BAG in 1 CASE (0487-4301-50) / 500 mL in 1 BAG
source: ndc

Packages (4)

Ingredients (1)

sodium chloride (9 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "49545dc2-5776-da02-e063-6394a90a7ef0", "openfda": {"upc": ["0304874301257", "0000000000000", "0304874301509", "0304874301059", "0304874301103"], "unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807632", "1807633", "1807634"], "spl_set_id": ["a4edf2d5-a9ff-30d4-e053-2995a90a5650"], "manufacturer_name": ["Nephron Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "64 BAG in 1 CASE (0487-4301-05)  / 50 mL in 1 BAG", "package_ndc": "0487-4301-05", "marketing_start_date": "20200604"}, {"sample": false, "description": "64 BAG in 1 CASE (0487-4301-10)  / 100 mL in 1 BAG", "package_ndc": "0487-4301-10", "marketing_start_date": "20200604"}, {"sample": false, "description": "35 BAG in 1 CASE (0487-4301-25)  / 250 mL in 1 BAG", "package_ndc": "0487-4301-25", "marketing_start_date": "20200604"}, {"sample": false, "description": "18 BAG in 1 CASE (0487-4301-50)  / 500 mL in 1 BAG", "package_ndc": "0487-4301-50", "marketing_start_date": "20200604"}], "brand_name": "Sodium Chloride", "product_id": "0487-4301_49545dc2-5776-da02-e063-6394a90a7ef0", "dosage_form": "INJECTION", "product_ndc": "0487-4301", "generic_name": "Sodium Chloride", "labeler_name": "Nephron Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "ANDA211968", "marketing_category": "ANDA", "marketing_start_date": "20200604", "listing_expiration_date": "20271231"}