Calcium Edetate de Sodium
- Product NDC
- 50633-320
- 11-digit product format
- 506330320
- Labeler code
- 50633
- Product ID
- 50633-320_d0da4fd6-f70e-4516-9036-2cf5dfbfe662
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- EDETATE CALCIUM DISODIUM ANHYDROUS
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- BTG International Inc
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Marketing start
- 2022-10-21
- Marketing end
- 0000-00-00
- Substance
- EDETATE CALCIUM DISODIUM ANHYDROUS
- Active strength
- 50 mg/mL
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50633-320-10 | 50633032010 | 10 mL in 1 CARTON (50633-320-10) | 10 ml | 2022-10-21 | 0000-00-00 | No | No | Current |