Product NDC: | 21695-500 |
Proprietary Name: | Diphenhydramine |
Non Proprietary Name: | Diphenhydramine |
Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-500 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20070101 |
Package NDC: | 21695-500-30 |
Package Description: | 30 CAPSULE in 1 BOTTLE (21695-500-30) |
NDC Code | 21695-500-30 |
Proprietary Name | Diphenhydramine |
Package Description | 30 CAPSULE in 1 BOTTLE (21695-500-30) |
Product NDC | 21695-500 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20070101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Rebel Distributors Corp |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |