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Phenobarbital
Phenobarbital - 63629-4026-2 - (Phenobarbital)
Drug Information of Phenobarbital
| Product NDC: | 63629-4026 |
| Proprietary Name: | Phenobarbital |
| Non Proprietary Name: | Phenobarbital |
| Active Ingredient(s): | 15 mg/1 & nbsp; Phenobarbital |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenobarbital
| Product NDC: | 63629-4026 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000101 |
Package Information of Phenobarbital
| Package NDC: | 63629-4026-2 |
| Package Description: | 15 TABLET in 1 BOTTLE (63629-4026-2) |
NDC Information of Phenobarbital
| NDC Code | 63629-4026-2 |
| Proprietary Name | Phenobarbital |
| Package Description | 15 TABLET in 1 BOTTLE (63629-4026-2) |
| Product NDC | 63629-4026 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenobarbital |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20000101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | PHENOBARBITAL |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
