| NDC Code | 66213-421-50 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (66213-421-50) |
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| Product NDC | 66213-421 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Donnatal Extentabs |
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| Non-Proprietary Name | Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20080507 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | PBM Pharmaceuticals, Inc |
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| Substance Name | PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE |
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| Strength | 48.6; .3111; .0582; .0195 |
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| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
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