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Imodium
Imodium - 50580-134-04 - (Loperamide Hydrochloride)
Drug Information of Imodium
| Product NDC: | 50580-134 |
| Proprietary Name: | Imodium |
| Non Proprietary Name: | Loperamide Hydrochloride |
| Active Ingredient(s): | 1 mg/7.5mL & nbsp; Loperamide Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Imodium
| Product NDC: | 50580-134 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019487 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050101 |
Package Information of Imodium
| Package NDC: | 50580-134-04 |
| Package Description: | 120 mL in 1 BOTTLE (50580-134-04) |
NDC Information of Imodium
| NDC Code | 50580-134-04 |
| Proprietary Name | Imodium |
| Package Description | 120 mL in 1 BOTTLE (50580-134-04) |
| Product NDC | 50580-134 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20050101 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/7.5mL |
| Pharmaceutical Classes |
