sodium chloride

Generic: sodium chloride

Labeler: henry schein, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler henry schein, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 4 meq/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9978
Product ID 0404-9978_5a2e919a-f17b-44eb-902b-daed3746f7e9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212248
Listing Expiration 2026-12-31
Marketing Start 2022-01-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049978
Hyphenated Format 0404-9978

Supplemental Identifiers

RxCUI
1807571
UNII
451W47IQ8X

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 ANDA212248 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 4 meq/mL
source: ndc
Packaging
  • 1 VIAL in 1 BAG (0404-9978-30) / 30 mL in 1 VIAL
source: ndc

Packages (1)

0404-9978-30 1 VIAL in 1 BAG (0404-9978-30) / 30 mL in 1 VIAL

Ingredients (1)

sodium chloride (4 meq/mL)

Linked Drug Pages (1)

SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "5a2e919a-f17b-44eb-902b-daed3746f7e9", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807571"], "spl_set_id": ["2e81ffca-05c6-4fa0-8911-4b3cbfa71351"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9978-30)  / 30 mL in 1 VIAL", "package_ndc": "0404-9978-30", "marketing_start_date": "20220112"}], "brand_name": "SODIUM CHLORIDE", "product_id": "0404-9978_5a2e919a-f17b-44eb-902b-daed3746f7e9", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "product_ndc": "0404-9978", "generic_name": "sodium chloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "4 meq/mL"}], "application_number": "ANDA212248", "marketing_category": "ANDA", "marketing_start_date": "20220112", "listing_expiration_date": "20261231"}