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Diphenhydramine Hydrochloride
Diphenhydramine Hydrochloride - 55154-9418-5 - (Diphenhydramine Hydrochloride)
Drug Information of Diphenhydramine Hydrochloride
| Product NDC: | 55154-9418 |
| Proprietary Name: | Diphenhydramine Hydrochloride |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 12.5 mg/5mL & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | ELIXIR |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine Hydrochloride
| Product NDC: | 55154-9418 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087513 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19820210 |
Package Information of Diphenhydramine Hydrochloride
| Package NDC: | 55154-9418-5 |
| Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-9418-5) > 5 mL in 1 CUP, UNIT-DOSE |
NDC Information of Diphenhydramine Hydrochloride
| NDC Code | 55154-9418-5 |
| Proprietary Name | Diphenhydramine Hydrochloride |
| Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-9418-5) > 5 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 55154-9418 |
| 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 | 12.5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
