Product NDC: | 41163-691 |
Proprietary Name: | Allergy |
Non Proprietary Name: | Diphenhydramine HCl |
Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41163-691 |
Labeler Name: | EQUALINE (SuperValu) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part336 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100722 |
Package NDC: | 41163-691-01 |
Package Description: | 1 BOTTLE in 1 BOX (41163-691-01) > 100 TABLET in 1 BOTTLE |
NDC Code | 41163-691-01 |
Proprietary Name | Allergy |
Package Description | 1 BOTTLE in 1 BOX (41163-691-01) > 100 TABLET in 1 BOTTLE |
Product NDC | 41163-691 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100722 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | EQUALINE (SuperValu) |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |