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Dexpanthenol
Dexpanthenol - 0517-0131-25 - (Dexpanthenol)
Drug Information of Dexpanthenol
| Product NDC: | 0517-0131 |
| Proprietary Name: | Dexpanthenol |
| Non Proprietary Name: | Dexpanthenol |
| Active Ingredient(s): | 250 mg/mL & nbsp; Dexpanthenol |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dexpanthenol
| Product NDC: | 0517-0131 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19930820 |
Package Information of Dexpanthenol
| Package NDC: | 0517-0131-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0131-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Dexpanthenol
| NDC Code | 0517-0131-25 |
| Proprietary Name | Dexpanthenol |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0131-25) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-0131 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dexpanthenol |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19930820 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | DEXPANTHENOL |
| Strength Number | 250 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
