| NDC Code | 68210-0099-2 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (68210-0099-2) / 24 TABLET in 1 BOTTLE |
|---|
| Product NDC | 68210-0099 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Extra Strength Pain Relief Pm |
|---|
| Non-Proprietary Name | Acetaminophen And Diphenhydramine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180410 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M013 |
|---|
| Manufacturer | Spirit Pharmaceutical LLC |
|---|
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
|---|
| Strength | 500; 25 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|