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Phenobarbital
Phenobarbital - 63739-201-10 - (Phenobarbital)
Drug Information of Phenobarbital
| Product NDC: | 63739-201 |
| Proprietary Name: | Phenobarbital |
| Non Proprietary Name: | Phenobarbital |
| Active Ingredient(s): | 32.4 mg/1 & nbsp; Phenobarbital |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenobarbital
| Product NDC: | 63739-201 |
| Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070717 |
Package Information of Phenobarbital
| Package NDC: | 63739-201-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-201-10) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Phenobarbital
| NDC Code | 63739-201-10 |
| Proprietary Name | Phenobarbital |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-201-10) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 63739-201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenobarbital |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070717 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
| Substance Name | PHENOBARBITAL |
| Strength Number | 32.4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
