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Loperamide Hydrochloride
Loperamide Hydrochloride - 46122-169-08 - (Loperamide Hydrochloride)
Drug Information of Loperamide Hydrochloride
| Product NDC: | 46122-169 |
| Proprietary Name: | Loperamide Hydrochloride |
| 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 Loperamide Hydrochloride
| Product NDC: | 46122-169 |
| Labeler Name: | Amerisource Bergen |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074091 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930201 |
Package Information of Loperamide Hydrochloride
| Package NDC: | 46122-169-08 |
| Package Description: | 72 TABLET in 1 BOTTLE (46122-169-08) |
NDC Information of Loperamide Hydrochloride
| NDC Code | 46122-169-08 |
| Proprietary Name | Loperamide Hydrochloride |
| Package Description | 72 TABLET in 1 BOTTLE (46122-169-08) |
| Product NDC | 46122-169 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19930201 |
| Marketing Category Name | ANDA |
| Labeler Name | Amerisource Bergen |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
