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Phenobarbital
Phenobarbital - 0603-5165-32 - (phenobarbital)
Drug Information of Phenobarbital
| Product NDC: | 0603-5165 |
| Proprietary Name: | Phenobarbital |
| Non Proprietary Name: | phenobarbital |
| Active Ingredient(s): | 16.2 mg/1 & nbsp; phenobarbital |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenobarbital
| Product NDC: | 0603-5165 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20020301 |
Package Information of Phenobarbital
| Package NDC: | 0603-5165-32 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5165-32) |
NDC Information of Phenobarbital
| NDC Code | 0603-5165-32 |
| Proprietary Name | Phenobarbital |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5165-32) |
| Product NDC | 0603-5165 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phenobarbital |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020301 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | PHENOBARBITAL |
| Strength Number | 16.2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
