Home
>
National Drug Code (NDC)
>
Imodium AD
Imodium AD - 66715-9720-1 - (Loperamide Hydrochloride)
Drug Information of Imodium AD
| Product NDC: | 66715-9720 |
| Proprietary Name: | Imodium AD |
| Non Proprietary Name: | Loperamide Hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Loperamide Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Imodium AD
| Product NDC: | 66715-9720 |
| Labeler Name: | Lil' Drug Store Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019860 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100510 |
Package Information of Imodium AD
| Package NDC: | 66715-9720-1 |
| Package Description: | 1 POUCH in 1 CARTON (66715-9720-1) > 2 TABLET, COATED in 1 POUCH |
NDC Information of Imodium AD
| NDC Code | 66715-9720-1 |
| Proprietary Name | Imodium AD |
| Package Description | 1 POUCH in 1 CARTON (66715-9720-1) > 2 TABLET, COATED in 1 POUCH |
| Product NDC | 66715-9720 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide Hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100510 |
| Marketing Category Name | NDA |
| Labeler Name | Lil' Drug Store Products, Inc. |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
