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Phenobarbital
Phenobarbital - 17856-1508-2 - (phenobarbital)
Drug Information of Phenobarbital
| Product NDC: | 17856-1508 |
| Proprietary Name: | Phenobarbital |
| Non Proprietary Name: | phenobarbital |
| Active Ingredient(s): | 20 mg/5mL & nbsp; phenobarbital |
| Administration Route(s): | ORAL |
| Dosage Form(s): | ELIXIR |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenobarbital
| Product NDC: | 17856-1508 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19970101 |
Package Information of Phenobarbital
| Package NDC: | 17856-1508-2 |
| Package Description: | 7.5 mL in 1 CUP (17856-1508-2) |
NDC Information of Phenobarbital
| NDC Code | 17856-1508-2 |
| Proprietary Name | Phenobarbital |
| Package Description | 7.5 mL in 1 CUP (17856-1508-2) |
| Product NDC | 17856-1508 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phenobarbital |
| Dosage Form Name | ELIXIR |
| Route Name | ORAL |
| Start Marketing Date | 19970101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | PHENOBARBITAL |
| Strength Number | 20 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
