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Loperamide Hydrochloride
Loperamide Hydrochloride - 50383-618-04 - (Loperamide Hydrochloride)
Drug Information of Loperamide Hydrochloride
| Product NDC: | 50383-618 |
| Proprietary Name: | Loperamide Hydrochloride |
| Non Proprietary Name: | Loperamide Hydrochloride |
| Active Ingredient(s): | 1 mg/5mL & nbsp; Loperamide Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Loperamide Hydrochloride
| Product NDC: | 50383-618 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074352 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19951117 |
Package Information of Loperamide Hydrochloride
| Package NDC: | 50383-618-04 |
| Package Description: | 1 BOTTLE in 1 CARTON (50383-618-04) > 118 mL in 1 BOTTLE |
NDC Information of Loperamide Hydrochloride
| NDC Code | 50383-618-04 |
| Proprietary Name | Loperamide Hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (50383-618-04) > 118 mL in 1 BOTTLE |
| Product NDC | 50383-618 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19951117 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
