Calcium Chloride
- Product NDC
- 0517-2710
- 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
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 |