Product NDC: | 11822-1645 |
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) |
Product NDC: | 11822-1645 |
Labeler Name: | Rite Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA091292 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120523 |
Package NDC: | 11822-1645-1 |
Package Description: | 120 mL in 1 BOTTLE (11822-1645-1) |
NDC Code | 11822-1645-1 |
Proprietary Name | loperamide hydrochloride |
Package Description | 120 mL in 1 BOTTLE (11822-1645-1) |
Product NDC | 11822-1645 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | loperamide HCl |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20120523 |
Marketing Category Name | ANDA |
Labeler Name | Rite Aid Corporation |
Substance Name | LOPERAMIDE HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/7.5mL |
Pharmaceutical Classes |