| NDC Code | 76237-149-39 |
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| Package Description | 30 TABLET in 1 BLISTER PACK (76237-149-39) |
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| Product NDC | 76237-149 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diphenoxylate Hydrochloride And Atropine Sulfate |
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| Non-Proprietary Name | Diphenoxylate Hydrochloride And Atropine Sulfate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20111107 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA085762 |
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| Manufacturer | McKesson Contract Packaging |
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| Substance Name | DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE |
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| Strength | 2.5; .025 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
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| DEA Schedule | CV |
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