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Dehydrated Alcohol
Dehydrated Alcohol - 17478-503-05 - (Alcohol)
Drug Information of Dehydrated Alcohol
| Product NDC: | 17478-503 |
| Proprietary Name: | Dehydrated Alcohol |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | .98 mL/mL & nbsp; Alcohol |
| Administration Route(s): | INTRASPINAL |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dehydrated Alcohol
| Product NDC: | 17478-503 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19970201 |
Package Information of Dehydrated Alcohol
| Package NDC: | 17478-503-05 |
| Package Description: | 10 VIAL in 1 CARTON (17478-503-05) > 5 mL in 1 VIAL |
NDC Information of Dehydrated Alcohol
| NDC Code | 17478-503-05 |
| Proprietary Name | Dehydrated Alcohol |
| Package Description | 10 VIAL in 1 CARTON (17478-503-05) > 5 mL in 1 VIAL |
| Product NDC | 17478-503 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | INJECTION |
| Route Name | INTRASPINAL |
| Start Marketing Date | 19970201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Akorn, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .98 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
