Product NDC: | 35356-865 |
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: | 35356-865 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20000501 |
Package NDC: | 35356-865-20 |
Package Description: | 20 CAPSULE in 1 BOTTLE (35356-865-20) |
NDC Code | 35356-865-20 |
Proprietary Name | diphenhydramine hydrochloride |
Package Description | 20 CAPSULE in 1 BOTTLE (35356-865-20) |
Product NDC | 35356-865 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | diphenhydramine hydrochloride |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20000501 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |