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Amytal Sodium
Amytal Sodium - 42998-303-01 - (amobarbital sodium)
Drug Information of Amytal Sodium
| Product NDC: | 42998-303 |
| Proprietary Name: | Amytal Sodium |
| Non Proprietary Name: | amobarbital sodium |
| Active Ingredient(s): | .5 g/5mL & nbsp; amobarbital sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amytal Sodium
| Product NDC: | 42998-303 |
| Labeler Name: | Marathon Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20080925 |
Package Information of Amytal Sodium
| Package NDC: | 42998-303-01 |
| Package Description: | 5 mL in 1 VIAL, GLASS (42998-303-01) |
NDC Information of Amytal Sodium
| NDC Code | 42998-303-01 |
| Proprietary Name | Amytal Sodium |
| Package Description | 5 mL in 1 VIAL, GLASS (42998-303-01) |
| Product NDC | 42998-303 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amobarbital sodium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20080925 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Marathon Pharmaceuticals, LLC |
| Substance Name | AMOBARBITAL SODIUM |
| Strength Number | .5 |
| Strength Unit | g/5mL |
| Pharmaceutical Classes |
