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Loperamide Hydrochloride
Loperamide Hydrochloride - 37808-645-26 - (loperamide HCl)
Drug Information of Loperamide Hydrochloride
| Product NDC: | 37808-645 |
| Proprietary Name: | Loperamide Hydrochloride |
| Non Proprietary Name: | loperamide HCl |
| Active Ingredient(s): | 1 mg/7.5mL & nbsp; loperamide HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Loperamide Hydrochloride
| Product NDC: | 37808-645 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091292 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120305 |
Package Information of Loperamide Hydrochloride
| Package NDC: | 37808-645-26 |
| Package Description: | 120 mL in 1 BOTTLE (37808-645-26) |
NDC Information of Loperamide Hydrochloride
| NDC Code | 37808-645-26 |
| Proprietary Name | Loperamide Hydrochloride |
| Package Description | 120 mL in 1 BOTTLE (37808-645-26) |
| Product NDC | 37808-645 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | loperamide HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120305 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/7.5mL |
| Pharmaceutical Classes |
