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Loperamide Hydrochloride
Loperamide Hydrochloride - 68094-217-62 - (Loperamide Hydrochloride)
Drug Information of Loperamide Hydrochloride
| Product NDC: | 68094-217 |
| Proprietary Name: | Loperamide Hydrochloride |
| Non Proprietary Name: | Loperamide Hydrochloride |
| Active Ingredient(s): | 2 mg/10mL & nbsp; Loperamide Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Loperamide Hydrochloride
| Product NDC: | 68094-217 |
| Labeler Name: | Precision Dose Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA073243 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090818 |
Package Information of Loperamide Hydrochloride
| Package NDC: | 68094-217-62 |
| Package Description: | 3 TRAY in 1 CASE (68094-217-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-217-59) |
NDC Information of Loperamide Hydrochloride
| NDC Code | 68094-217-62 |
| Proprietary Name | Loperamide Hydrochloride |
| Package Description | 3 TRAY in 1 CASE (68094-217-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-217-59) |
| Product NDC | 68094-217 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090818 |
| Marketing Category Name | ANDA |
| Labeler Name | Precision Dose Inc. |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes |
