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IMODIUM
IMODIUM - 50580-295-06 - (Loperamide hydrochloride)
Drug Information of IMODIUM
| Product NDC: | 50580-295 |
| Proprietary Name: | IMODIUM |
| Non Proprietary Name: | Loperamide hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Loperamide hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IMODIUM
| Product NDC: | 50580-295 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019860 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19891201 |
Package Information of IMODIUM
| Package NDC: | 50580-295-06 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (50580-295-06) > 6 TABLET in 1 BLISTER PACK |
NDC Information of IMODIUM
| NDC Code | 50580-295-06 |
| Proprietary Name | IMODIUM |
| Package Description | 1 BLISTER PACK in 1 CARTON (50580-295-06) > 6 TABLET in 1 BLISTER PACK |
| Product NDC | 50580-295 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19891201 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
