Home NDC 72819-235 CHROMIC CHLORIDE
Product NDC 72819-235
11-digit product format 728190235
Labeler code 72819
Product ID 72819-235_2c77c922-0469-6bfd-e063-6394a90a48ea
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name CHROMIC CHLORIDE
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler Archis Pharma LLC
Application ANDA218538
Marketing category ANDA
Marketing start 2025-01-25
Substance CHROMIC CHLORIDE
Active strength 4 ug/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A218538-001 CHROMIC CHLORIDE CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A218538-001 AP
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-02-19 14:30 UTC 2026-02 A218538-001 CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A218538-001 CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A218538-001 CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A218538-001 CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A218538-001 CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A218538-001 CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A218538-001 CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18 2680178bc6a6…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A218538-001 CHROMIC CHLORIDE EQ 0.004MG CHROMIUM/ML INJECTABLE / INJECTION AP 2024-11-18 a50c72e98297…
Observed Orange Book normalized TE history# Additional Listing Data#
Finished product Yes
Brand name base CHROMIC CHLORIDE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHROMIC CHLORIDE 4 ug/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination KB1PCR9DMW Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 204401 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72819-235-06 CHROMIC CHLORIDE 10 mL in 1 VIAL, SINGLE-DOSE INJECTION, SOLUTION 10 2 72819-235-16 CHROMIC CHLORIDE 25 in 1 PACKAGE INJECTION, SOLUTION 25 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72819-235 CHROMIC CHLORIDE INJECTION, SOLUTION [ARCHIS PHARMA LLC] 2 Current NDC, 2 package rows 20250125_db372536-fd36-4596-91d1-5ad72d748c41.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72819-235-06 72819023506 10 mL in 1 VIAL, SINGLE-DOSE 10 ml Historical 72819-235-16 72819023516 25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-235-16) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-235-06) 2025-01-25 No No Current