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Butisol Sodium
Butisol Sodium - 0037-0113-60 - (Butabarbital Sodium)
Drug Information of Butisol Sodium
| Product NDC: | 0037-0113 |
| Proprietary Name: | Butisol Sodium |
| Non Proprietary Name: | Butabarbital Sodium |
| Active Ingredient(s): | 30 mg/1 & nbsp; Butabarbital Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Butisol Sodium
| Product NDC: | 0037-0113 |
| Labeler Name: | Meda Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA000793 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19390801 |
Package Information of Butisol Sodium
| Package NDC: | 0037-0113-60 |
| Package Description: | 100 TABLET in 1 BOTTLE (0037-0113-60) |
NDC Information of Butisol Sodium
| NDC Code | 0037-0113-60 |
| Proprietary Name | Butisol Sodium |
| Package Description | 100 TABLET in 1 BOTTLE (0037-0113-60) |
| Product NDC | 0037-0113 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Butabarbital Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19390801 |
| Marketing Category Name | NDA |
| Labeler Name | Meda Pharmaceuticals Inc. |
| Substance Name | BUTABARBITAL SODIUM |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
