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Chromic Chloride
Chromic Chloride - 0517-6310-25 - (Chromic Chloride)
Drug Information of Chromic Chloride
| Product NDC: | 0517-6310 |
| Proprietary Name: | Chromic Chloride |
| Non Proprietary Name: | Chromic Chloride |
| Active Ingredient(s): | 20.5 ug/mL & nbsp; Chromic Chloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chromic Chloride
| Product NDC: | 0517-6310 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900930 |
Package Information of Chromic Chloride
| Package NDC: | 0517-6310-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-6310-25) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Chromic Chloride
| NDC Code | 0517-6310-25 |
| Proprietary Name | Chromic Chloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-6310-25) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-6310 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chromic Chloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19900930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | CHROMIC CHLORIDE |
| Strength Number | 20.5 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient] |
