Calcium Disodium Versenate
- Product NDC
- 99207-240
- 11-digit product format
- 992070240
- Labeler code
- 99207
- Product ID
- 99207-240_c3e61446-06de-4a15-8a6a-830fa6e8b2ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- EDETATE CALCIUM DISODIUM
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Bausch Health Us, LLC
- Application
- NDA008922
- Marketing category
- NDA
- Marketing start
- 2013-06-21
- Marketing end
- 0000-00-00
- Substance
- EDETATE CALCIUM DISODIUM
- Active strength
- 200 mg/mL
- Pharmacologic classes
- Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Lead Chelating Activity [MoA],Lead Chelator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 99207-240-05 | 99207024005 | 5 AMPULE in 1 CARTON (99207-240-05) > 5 mL in 1 AMPULE | 5 ampule | 2016-06-21 | 0000-00-00 | No | No | Current |