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Donnatal
Donnatal - 66213-422-16 - (phenobarbital elixir)
Drug Information of Donnatal
| Product NDC: | 66213-422 |
| Proprietary Name: | Donnatal |
| Non Proprietary Name: | phenobarbital elixir |
| Active Ingredient(s): | .0194; .1037; 16.2; .0065 mg/5mL; mg/5mL; mg/5mL; mg/5mL & nbsp; phenobarbital elixir |
| Administration Route(s): | ORAL |
| Dosage Form(s): | ELIXIR |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Donnatal
| Product NDC: | 66213-422 |
| Labeler Name: | PBM Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110701 |
Package Information of Donnatal
| Package NDC: | 66213-422-16 |
| Package Description: | 470 mL in 1 BOTTLE (66213-422-16) |
NDC Information of Donnatal
| NDC Code | 66213-422-16 |
| Proprietary Name | Donnatal |
| Package Description | 470 mL in 1 BOTTLE (66213-422-16) |
| Product NDC | 66213-422 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phenobarbital elixir |
| Dosage Form Name | ELIXIR |
| Route Name | ORAL |
| Start Marketing Date | 20110701 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | PBM Pharmaceuticals Inc. |
| Substance Name | ATROPINE SULFATE; HYOSCYAMINE SULFATE; PHENOBARBITAL; SCOPOLAMINE HYDROBROMIDE |
| Strength Number | .0194; .1037; 16.2; .0065 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
