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Phenobarbital
Phenobarbital - 0463-6151-01 - (Phenobarbital)
Drug Information of Phenobarbital
| Product NDC: | 0463-6151 |
| Proprietary Name: | Phenobarbital |
| Non Proprietary Name: | Phenobarbital |
| Active Ingredient(s): | 60 mg/1 & nbsp; Phenobarbital |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenobarbital
| Product NDC: | 0463-6151 |
| Labeler Name: | C.O. Truxton, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120301 |
Package Information of Phenobarbital
| Package NDC: | 0463-6151-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0463-6151-01) |
NDC Information of Phenobarbital
| NDC Code | 0463-6151-01 |
| Proprietary Name | Phenobarbital |
| Package Description | 100 TABLET in 1 BOTTLE (0463-6151-01) |
| Product NDC | 0463-6151 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenobarbital |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | C.O. Truxton, Inc. |
| Substance Name | PHENOBARBITAL |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
