| NDC Code | 50269-552-01 |
|---|
| Package Description | 20 POUCH in 1 BOX (50269-552-01) / 2 TABLET, FILM COATED in 1 POUCH |
|---|
| Product NDC | 50269-552 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Tylenol Pm |
|---|
| Non-Proprietary Name | Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160711 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M013 |
|---|
| Manufacturer | JC World Bell Wholesale Co., Inc. |
|---|
| 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] |
|---|