Product NDC: | 0037-0110 |
Proprietary Name: | Butisol Sodium |
Non Proprietary Name: | Butabarbital Sodium |
Active Ingredient(s): | 30 mg/5mL & nbsp; Butabarbital Sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0037-0110 |
Labeler Name: | Meda Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA085380 |
Marketing Category: | ANDA |
Start Marketing Date: | 19780601 |
Package NDC: | 0037-0110-16 |
Package Description: | 473 mL in 1 BOTTLE (0037-0110-16) |
NDC Code | 0037-0110-16 |
Proprietary Name | Butisol Sodium |
Package Description | 473 mL in 1 BOTTLE (0037-0110-16) |
Product NDC | 0037-0110 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Butabarbital Sodium |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19780601 |
Marketing Category Name | ANDA |
Labeler Name | Meda Pharmaceuticals Inc. |
Substance Name | BUTABARBITAL SODIUM |
Strength Number | 30 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |