| NDC Code | 17714-135-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (17714-135-01) |
|---|
| Product NDC | 17714-135 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Diphenhydramine Hydrochloride |
|---|
| Non-Proprietary Name | Diphenhydramine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20060926 |
|---|
| Marketing Category Name | OTC MONOGRAPH FINAL |
|---|
| Application Number | part341 |
|---|
| Manufacturer | Advance Pharmaceutical Inc. |
|---|
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|