Product NDC: | 55154-9409 |
Proprietary Name: | Diphenhydramine Hydrochloride |
Non Proprietary Name: | Diphenhydramine Hydrochloride |
Active Ingredient(s): | 25 mg/10mL & nbsp; Diphenhydramine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | ELIXIR |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-9409 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087513 |
Marketing Category: | ANDA |
Start Marketing Date: | 19820210 |
Package NDC: | 55154-9409-5 |
Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-9409-5) > 10 mL in 1 CUP, UNIT-DOSE |
NDC Code | 55154-9409-5 |
Proprietary Name | Diphenhydramine Hydrochloride |
Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-9409-5) > 10 mL in 1 CUP, UNIT-DOSE |
Product NDC | 55154-9409 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diphenhydramine Hydrochloride |
Dosage Form Name | ELIXIR |
Route Name | ORAL |
Start Marketing Date | 19820210 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |