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Motofen
Motofen - 0187-0500-02 - (difenoxin hydrochloride)
Drug Information of Motofen
| Product NDC: | 0187-0500 |
| Proprietary Name: | Motofen |
| Non Proprietary Name: | difenoxin hydrochloride |
| Active Ingredient(s): | .025; 1 mg/1; mg/1 & nbsp; difenoxin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Motofen
| Product NDC: | 0187-0500 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017744 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19620714 |
Package Information of Motofen
| Package NDC: | 0187-0500-02 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0187-0500-02) |
NDC Information of Motofen
| NDC Code | 0187-0500-02 |
| Proprietary Name | Motofen |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0187-0500-02) |
| Product NDC | 0187-0500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | difenoxin hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19620714 |
| Marketing Category Name | NDA |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE |
| Strength Number | .025; 1 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
