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Donnatal Extentabs
Donnatal Extentabs - 65084-450-10 - (Phenobarbitol)
Drug Information of Donnatal Extentabs
| Product NDC: | 65084-450 |
| Proprietary Name: | Donnatal Extentabs |
| Non Proprietary Name: | Phenobarbitol |
| Active Ingredient(s): | .0582; .3111; 48.6; .0195 mg/1; mg/1; mg/1; mg/1 & nbsp; Phenobarbitol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Donnatal Extentabs
| Product NDC: | 65084-450 |
| Labeler Name: | RxPak Division of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110727 |
Package Information of Donnatal Extentabs
| Package NDC: | 65084-450-10 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65084-450-10) |
NDC Information of Donnatal Extentabs
| NDC Code | 65084-450-10 |
| Proprietary Name | Donnatal Extentabs |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65084-450-10) |
| Product NDC | 65084-450 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenobarbitol |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110727 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | RxPak Division of McKesson Corporation |
| Substance Name | ATROPINE SULFATE; HYOSCYAMINE; PHENOBARBITAL; SCOPOLAMINE HYDROBROMIDE |
| Strength Number | .0582; .3111; 48.6; .0195 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
