Product NDC: | 42507-224 |
Proprietary Name: | anti diarrheal |
Non Proprietary Name: | Loperamide Hydrochloride |
Active Ingredient(s): | 2 mg/1 & nbsp; Loperamide Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42507-224 |
Labeler Name: | HyVee Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075232 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030321 |
Package NDC: | 42507-224-80 |
Package Description: | 1 BOTTLE in 1 CARTON (42507-224-80) > 96 TABLET, FILM COATED in 1 BOTTLE |
NDC Code | 42507-224-80 |
Proprietary Name | anti diarrheal |
Package Description | 1 BOTTLE in 1 CARTON (42507-224-80) > 96 TABLET, FILM COATED in 1 BOTTLE |
Product NDC | 42507-224 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Loperamide Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20030321 |
Marketing Category Name | ANDA |
Labeler Name | HyVee Inc |
Substance Name | LOPERAMIDE HYDROCHLORIDE |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes |