Product NDC: | 42254-190 |
Proprietary Name: | Diphenhydramine Hydrochloride |
Non Proprietary Name: | diphenhydramine hydrochloride |
Active Ingredient(s): | 50 mg/mL & nbsp; diphenhydramine hydrochloride |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42254-190 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA080817 |
Marketing Category: | ANDA |
Start Marketing Date: | 19721127 |
Package NDC: | 42254-190-01 |
Package Description: | 25 VIAL in 1 PACKAGE (42254-190-01) > 1 mL in 1 VIAL |
NDC Code | 42254-190-01 |
Proprietary Name | Diphenhydramine Hydrochloride |
Package Description | 25 VIAL in 1 PACKAGE (42254-190-01) > 1 mL in 1 VIAL |
Product NDC | 42254-190 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diphenhydramine hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 19721127 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |