| NDC Code | 0641-0376-25 |
|---|
| Package Description | 25 VIAL in 1 PACKAGE (0641-0376-25) / 1 mL in 1 VIAL (0641-0376-21) |
|---|
| Product NDC | 0641-0376 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diphenhydramine Hydrochloride |
|---|
| Non-Proprietary Name | Diphenhydramine Hydrochloride |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 19721127 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA080817 |
|---|
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|