chromic chloride

Generic: chromic chloride

Labeler: archis pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chromic chloride
Generic Name chromic chloride
Labeler archis pharma llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

chromic chloride 4 ug/mL

Manufacturer
Archis Pharma LLC

Identifiers & Regulatory

Product NDC 72819-235
Product ID 72819-235_2c77c922-0469-6bfd-e063-6394a90a48ea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218538
Listing Expiration 2026-12-31
Marketing Start 2025-01-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72819235
Hyphenated Format 72819-235

Supplemental Identifiers

RxCUI
204401
UPC
0372819235165
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 chromic chloride (source: ndc)
Generic Name chromic chloride (source: ndc)
Application Number ANDA218538 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 4 ug/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-235-16) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-235-06)
source: ndc

Packages (1)

Ingredients (1)

chromic chloride (4 ug/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2c77c922-0469-6bfd-e063-6394a90a48ea", "openfda": {"upc": ["0372819235165"], "unii": ["KB1PCR9DMW"], "rxcui": ["204401"], "spl_set_id": ["db372536-fd36-4596-91d1-5ad72d748c41"], "manufacturer_name": ["Archis Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-235-16)  / 10 mL in 1 VIAL, SINGLE-DOSE (72819-235-06)", "package_ndc": "72819-235-16", "marketing_start_date": "20250125"}], "brand_name": "CHROMIC CHLORIDE", "product_id": "72819-235_2c77c922-0469-6bfd-e063-6394a90a48ea", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "72819-235", "generic_name": "CHROMIC CHLORIDE", "labeler_name": "Archis Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHROMIC CHLORIDE", "active_ingredients": [{"name": "CHROMIC CHLORIDE", "strength": "4 ug/mL"}], "application_number": "ANDA218538", "marketing_category": "ANDA", "marketing_start_date": "20250125", "listing_expiration_date": "20261231"}