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Phenobarbital
Phenobarbital - 76237-222-39 - (Phenobarbital)
Drug Information of Phenobarbital
| Product NDC: | 76237-222 |
| 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: | 76237-222 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120220 |
Package Information of Phenobarbital
| Package NDC: | 76237-222-39 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (76237-222-39) |
NDC Information of Phenobarbital
| NDC Code | 76237-222-39 |
| Proprietary Name | Phenobarbital |
| Package Description | 30 TABLET in 1 BLISTER PACK (76237-222-39) |
| Product NDC | 76237-222 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenobarbital |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120220 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | McKesson Contract Packaging |
| Substance Name | PHENOBARBITAL |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
