Product NDC: | 55154-4944 |
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) |
Product NDC: | 55154-4944 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA073079 |
Marketing Category: | ANDA |
Start Marketing Date: | 19920430 |
Package NDC: | 55154-4944-5 |
Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-4944-5) > 10 mL in 1 CUP, UNIT-DOSE |
NDC Code | 55154-4944-5 |
Proprietary Name | Loperamide Hydrochloride |
Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-4944-5) > 10 mL in 1 CUP, UNIT-DOSE |
Product NDC | 55154-4944 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Loperamide Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19920430 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | LOPERAMIDE HYDROCHLORIDE |
Strength Number | 2 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |