| Product NDC: | 59779-645 | 
| Proprietary Name: | loperamide hydrochloride | 
| Non Proprietary Name: | loperamide HCl | 
| Active Ingredient(s): | 1 mg/7.5mL & nbsp; loperamide HCl | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-645 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA091292 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20120228 | 
| Package NDC: | 59779-645-26 | 
| Package Description: | 1 BOTTLE in 1 CARTON (59779-645-26) > 120 mL in 1 BOTTLE | 
| NDC Code | 59779-645-26 | 
| Proprietary Name | loperamide hydrochloride | 
| Package Description | 1 BOTTLE in 1 CARTON (59779-645-26) > 120 mL in 1 BOTTLE | 
| Product NDC | 59779-645 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | loperamide HCl | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20120228 | 
| Marketing Category Name | ANDA | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | LOPERAMIDE HYDROCHLORIDE | 
| Strength Number | 1 | 
| Strength Unit | mg/7.5mL | 
| Pharmaceutical Classes |