| NDC Code | 0187-0500-02 | 
|---|
			| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0187-0500-02) | 
|---|
			| Product NDC | 0187-0500 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Motofen | 
|---|
			
			| Non-Proprietary Name | Difenoxin Hydrochloride | 
|---|
			| Dosage Form | TABLET | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 19620714 | 
|---|
			| End Marketing Date | 20141130 | 
|---|
			| Marketing Category Name | NDA | 
|---|
			| Application Number | NDA017744 | 
|---|
			| Manufacturer | Valeant Pharmaceuticals North America LLC | 
|---|
			| Substance Name | ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE | 
|---|
			| Strength | .025; 1 | 
|---|
			| Strength Unit | mg/1; mg/1 | 
|---|
			| Pharmacy Classes | Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] | 
|---|
			| DEA Schedule | CIV | 
|---|