Product NDC: | 0904-5306 |
Proprietary Name: | Diphenhydramine Hydrochloride |
Non Proprietary Name: | Diphenhydramine Hydrochloride |
Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-5306 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090102 |
Package NDC: | 0904-5306-61 |
Package Description: | 100 CAPSULE in 1 BOX, UNIT-DOSE (0904-5306-61) |
NDC Code | 0904-5306-61 |
Proprietary Name | Diphenhydramine Hydrochloride |
Package Description | 100 CAPSULE in 1 BOX, UNIT-DOSE (0904-5306-61) |
Product NDC | 0904-5306 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine Hydrochloride |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20090102 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Major Pharmaceuticals |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |