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Phenobarbital
Phenobarbital - 16571-330-16 - (Phenobarbital)
Drug Information of Phenobarbital
| Product NDC: | 16571-330 |
| Proprietary Name: | Phenobarbital |
| Non Proprietary Name: | Phenobarbital |
| Active Ingredient(s): | 20 mg/5mL & nbsp; Phenobarbital |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenobarbital
| Product NDC: | 16571-330 |
| Labeler Name: | Pack Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110708 |
Package Information of Phenobarbital
| Package NDC: | 16571-330-16 |
| Package Description: | 473 mL in 1 BOTTLE (16571-330-16) |
NDC Information of Phenobarbital
| NDC Code | 16571-330-16 |
| Proprietary Name | Phenobarbital |
| Package Description | 473 mL in 1 BOTTLE (16571-330-16) |
| Product NDC | 16571-330 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenobarbital |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110708 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Pack Pharmaceuticals, LLC |
| Substance Name | PHENOBARBITAL |
| Strength Number | 20 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
