Product NDC: | 37808-377 |
Proprietary Name: | rx act anti diarrheal |
Non Proprietary Name: | Loperamide HCl |
Active Ingredient(s): | 1 mg/5mL & nbsp; Loperamide HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37808-377 |
Labeler Name: | H E B |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA073243 |
Marketing Category: | ANDA |
Start Marketing Date: | 19920514 |
Package NDC: | 37808-377-26 |
Package Description: | 1 BOTTLE in 1 CARTON (37808-377-26) > 120 mL in 1 BOTTLE |
NDC Code | 37808-377-26 |
Proprietary Name | rx act anti diarrheal |
Package Description | 1 BOTTLE in 1 CARTON (37808-377-26) > 120 mL in 1 BOTTLE |
Product NDC | 37808-377 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Loperamide HCl |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19920514 |
Marketing Category Name | ANDA |
Labeler Name | H E B |
Substance Name | LOPERAMIDE HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |