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Lomotil
Lomotil - 0025-0061-34 - (diphenoxylate hydrochloride and atropine sulfate)
Drug Information of Lomotil
| Product NDC: | 0025-0061 |
| Proprietary Name: | Lomotil |
| Non Proprietary Name: | diphenoxylate hydrochloride and atropine sulfate |
| Active Ingredient(s): | .025; 2.5 mg/1; mg/1 & nbsp; diphenoxylate hydrochloride and atropine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lomotil
| Product NDC: | 0025-0061 |
| Labeler Name: | G.D. Searle LLC Division of Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012462 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19600915 |
Package Information of Lomotil
| Package NDC: | 0025-0061-34 |
| Package Description: | 100 TABLET in 1 CARTON (0025-0061-34) |
NDC Information of Lomotil
| NDC Code | 0025-0061-34 |
| Proprietary Name | Lomotil |
| Package Description | 100 TABLET in 1 CARTON (0025-0061-34) |
| Product NDC | 0025-0061 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diphenoxylate hydrochloride and atropine sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19600915 |
| Marketing Category Name | NDA |
| Labeler Name | G.D. Searle LLC Division of Pfizer Inc |
| Substance Name | ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE |
| Strength Number | .025; 2.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
