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Dayhist allergy
Dayhist allergy - 42507-282-51 - (Clemastine fumarate)
Drug Information of Dayhist allergy
| Product NDC: | 42507-282 |
| Proprietary Name: | Dayhist allergy |
| Non Proprietary Name: | Clemastine fumarate |
| Active Ingredient(s): | 1.34 mg/1 & nbsp; Clemastine fumarate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dayhist allergy
| Product NDC: | 42507-282 |
| Labeler Name: | HyVee Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074512 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960621 |
Package Information of Dayhist allergy
| Package NDC: | 42507-282-51 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (42507-282-51) > 8 TABLET in 1 BLISTER PACK |
NDC Information of Dayhist allergy
| NDC Code | 42507-282-51 |
| Proprietary Name | Dayhist allergy |
| Package Description | 1 BLISTER PACK in 1 CARTON (42507-282-51) > 8 TABLET in 1 BLISTER PACK |
| Product NDC | 42507-282 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clemastine fumarate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960621 |
| Marketing Category Name | ANDA |
| Labeler Name | HyVee Inc |
| Substance Name | CLEMASTINE FUMARATE |
| Strength Number | 1.34 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
