Product NDC: | 47682-184 |
Proprietary Name: | Medique Diphen |
Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient(s): | 25 mg/1 & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47682-184 |
Labeler Name: | Unifirst First Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120101 |
Package NDC: | 47682-184-32 |
Package Description: | 12 PACKET in 1 BOX, UNIT-DOSE (47682-184-32) > 1 TABLET, FILM COATED in 1 PACKET (47682-184-46) (47682-184-46) |
NDC Code | 47682-184-32 |
Proprietary Name | Medique Diphen |
Package Description | 12 PACKET in 1 BOX, UNIT-DOSE (47682-184-32) > 1 TABLET, FILM COATED in 1 PACKET (47682-184-46) (47682-184-46) |
Product NDC | 47682-184 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Unifirst First Aid Corporation |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |