Product NDC: | 59779-479 |
Proprietary Name: | allergy |
Non Proprietary Name: | Diphenhydramine Hydrochloride |
Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-479 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19910814 |
Package NDC: | 59779-479-68 |
Package Description: | 3 BLISTER PACK in 1 CARTON (59779-479-68) > 12 TABLET in 1 BLISTER PACK |
NDC Code | 59779-479-68 |
Proprietary Name | allergy |
Package Description | 3 BLISTER PACK in 1 CARTON (59779-479-68) > 12 TABLET in 1 BLISTER PACK |
Product NDC | 59779-479 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19910814 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |