NDC Code | 70518-1082-1 |
Package Description | 25 VIAL in 1 PACKAGE (70518-1082-1) / 1 mL in 1 VIAL (70518-1082-0) |
Product NDC | 70518-1082 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Diphenhydramine Hydrochloride |
Non-Proprietary Name | Diphenhydramine Hydrochloride |
Dosage Form | INJECTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20180327 |
Marketing Category Name | ANDA |
Application Number | ANDA080817 |
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] |