 
                        | Product NDC: | 55312-960 | 
| Proprietary Name: | a d | 
| Non Proprietary Name: | Loperamide HCl | 
| Active Ingredient(s): | 2 mg/1 & nbsp; Loperamide HCl | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 55312-960 | 
| Labeler Name: | Western Family Foods Inc | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA075232 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20030410 | 
| Package NDC: | 55312-960-89 | 
| Package Description: | 3 BLISTER PACK in 1 CARTON (55312-960-89) > 6 TABLET, FILM COATED in 1 BLISTER PACK | 
| NDC Code | 55312-960-89 | 
| Proprietary Name | a d | 
| Package Description | 3 BLISTER PACK in 1 CARTON (55312-960-89) > 6 TABLET, FILM COATED in 1 BLISTER PACK | 
| Product NDC | 55312-960 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Loperamide HCl | 
| Dosage Form Name | TABLET, FILM COATED | 
| Route Name | ORAL | 
| Start Marketing Date | 20030410 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Western Family Foods Inc | 
| Substance Name | LOPERAMIDE HYDROCHLORIDE | 
| Strength Number | 2 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes |