| NDC Code | 51662-1348-1 |
|---|
| Package Description | 1 mL in 1 VIAL (51662-1348-1) |
|---|
| Product NDC | 51662-1348 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Diphenhydramine Hydrochloride |
|---|
| Non-Proprietary Name | Diphenhydramine Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20181126 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040466 |
|---|
| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
|---|
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|