NDC Code | 70518-3685-0 |
Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (70518-3685-0) / 1 mL in 1 VIAL, SINGLE-DOSE (70518-3685-1) |
Product NDC | 70518-3685 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Diphenhydramine |
Non-Proprietary Name | Diphenhydramine Hydrochloride |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20230320 |
Marketing Category Name | ANDA |
Application Number | ANDA040466 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength | 50 |
Strength Unit | mg/mL |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |