Home NDC 0517-2710-25 Calcium Chloride
Product NDC 0517-2710
Requested package NDC 0517-2710-25
11-digit product format 005172710
Labeler code 0517
Product ID 0517-2710_4420641e-3ccc-49ae-95c4-67febed94b13
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Calcium Chloride
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler American Regent, Inc.
Marketing category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start 2017-07-05
Marketing end 0000-00-00
Substance CALCIUM CHLORIDE
Active strength 100 mg/mL
Pharmacologic classes Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS]
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CALCIUM CHLORIDE ACTIVE INGREDIENT M4I0D6VV5M CALCIUM CHLORIDE INJECTION, SOLUTION [AMERICAN REGENT, INC.] 1 CALCIUM ACTIVE MOIETY SY7Q814VUP CALCIUM CHLORIDE INJECTION, SOLUTION [AMERICAN REGENT, INC.] 1 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB CALCIUM CHLORIDE INJECTION, SOLUTION [AMERICAN REGENT, INC.] 1 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I CALCIUM CHLORIDE INJECTION, SOLUTION [AMERICAN REGENT, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R CALCIUM CHLORIDE INJECTION, SOLUTION [AMERICAN REGENT, INC.] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0517-2710-25 00517271025 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2710-25) > 10 mL in 1 VIAL, SINGLE-DOSE 2017-07-05 0000-00-00 No No Current