Calcium Gluconate
- Product NDC
- 0517-3950
- 11-digit product format
- 005173950
- Labeler code
- 0517
- Product ID
- 0517-3950_5178d569-7ff6-46de-a8ce-498e9608ef3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Calcium Gluconate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- American Regent, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- CALCIUM GLUCONATE MONOHYDRATE
- Active strength
- 98 mg/mL
- Pharmacologic classes
- Calcium [CS],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#