chromium

Generic: chromic chloride

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name chromium
Generic Name chromic chloride
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

chromic chloride 4 ug/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-4093
Product ID 0409-4093_c4cf0833-1da8-43a6-8705-8a05433bb174
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018961
Listing Expiration 2026-12-31
Marketing Start 2016-04-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04094093
Hyphenated Format 0409-4093

Supplemental Identifiers

RxCUI
204401
UNII
KB1PCR9DMW

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 chromium (source: ndc)
Generic Name chromic chloride (source: ndc)
Application Number NDA018961 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 4 ug/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4093-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4093-09)
source: ndc

Packages (1)

Ingredients (1)

chromic chloride (4 ug/mL)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c4cf0833-1da8-43a6-8705-8a05433bb174", "openfda": {"unii": ["KB1PCR9DMW"], "rxcui": ["204401"], "spl_set_id": ["da207ca8-7836-4c66-92fe-36cc89baf773"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4093-10)  / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4093-09)", "package_ndc": "0409-4093-10", "marketing_start_date": "20160427"}], "brand_name": "Chromium", "product_id": "0409-4093_c4cf0833-1da8-43a6-8705-8a05433bb174", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0409-4093", "generic_name": "Chromic Chloride", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chromium", "active_ingredients": [{"name": "CHROMIC CHLORIDE", "strength": "4 ug/mL"}], "application_number": "NDA018961", "marketing_category": "NDA", "marketing_start_date": "20160427", "listing_expiration_date": "20261231"}