Product NDC: | 67457-124 |
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, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67457-124 |
Labeler Name: | Mylan Institutional LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040498 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130509 |
Package NDC: | 67457-124-10 |
Package Description: | 1 VIAL, GLASS in 1 CARTON (67457-124-10) > 10 mL in 1 VIAL, GLASS |
NDC Code | 67457-124-10 |
Proprietary Name | Diphenhydramine Hydrochloride |
Package Description | 1 VIAL, GLASS in 1 CARTON (67457-124-10) > 10 mL in 1 VIAL, GLASS |
Product NDC | 67457-124 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diphenhydramine hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20130509 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Institutional LLC |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |