| Product NDC: | 41163-375 |
| Proprietary Name: | Anti-Diarrheal |
| Non Proprietary Name: | Loperamides |
| Active Ingredient(s): | 2 mg/1 & nbsp; Loperamides |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 41163-375 |
| Labeler Name: | SUPERVALU INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076497 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050503 |
| Package NDC: | 41163-375-22 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (41163-375-22) > 48 TABLET in 1 BLISTER PACK |
| NDC Code | 41163-375-22 |
| Proprietary Name | Anti-Diarrheal |
| Package Description | 1 BLISTER PACK in 1 CARTON (41163-375-22) > 48 TABLET in 1 BLISTER PACK |
| Product NDC | 41163-375 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamides |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050503 |
| Marketing Category Name | ANDA |
| Labeler Name | SUPERVALU INC. |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |