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a d
a d - 55312-224-67 - (Loperamide Hydrochloride)
Drug Information of a d
| Product NDC: | 55312-224 |
| Proprietary Name: | a d |
| 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) |
Labeler Information of a d
| Product NDC: | 55312-224 |
| Labeler Name: | Western Family Foods Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075232 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030225 |
Package Information of a d
| Package NDC: | 55312-224-67 |
| Package Description: | 1 BOTTLE in 1 CARTON (55312-224-67) > 48 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of a d
| NDC Code | 55312-224-67 |
| Proprietary Name | a d |
| Package Description | 1 BOTTLE in 1 CARTON (55312-224-67) > 48 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 55312-224 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030225 |
| Marketing Category Name | ANDA |
| Labeler Name | Western Family Foods Inc |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
