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Dehydrated Alcohol
Dehydrated Alcohol - 0517-8571-10 - (Dehydrated Alcohol)
Drug Information of Dehydrated Alcohol
| Product NDC: | 0517-8571 |
| Proprietary Name: | Dehydrated Alcohol |
| Non Proprietary Name: | Dehydrated Alcohol |
| Active Ingredient(s): | .98 mL/mL & nbsp; Dehydrated Alcohol |
| Administration Route(s): | INTRASPINAL |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dehydrated Alcohol
| Product NDC: | 0517-8571 |
| 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 Dehydrated Alcohol
| Package NDC: | 0517-8571-10 |
| Package Description: | 10 AMPULE in 1 BOX (0517-8571-10) > 1 mL in 1 AMPULE |
NDC Information of Dehydrated Alcohol
| NDC Code | 0517-8571-10 |
| Proprietary Name | Dehydrated Alcohol |
| Package Description | 10 AMPULE in 1 BOX (0517-8571-10) > 1 mL in 1 AMPULE |
| Product NDC | 0517-8571 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dehydrated Alcohol |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRASPINAL |
| Start Marketing Date | 19900930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .98 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
