Product ID | 68210-4236_edae483f-10e3-5a71-e053-2a95a90a1b9c |
NDC | 68210-4236 |
Product Type | Human Otc Drug |
Proprietary Name | Pain Reliever and Sleep Aid |
Generic Name | Acetaminophen, And Diphenhydramine Hydrochloride |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2022-11-17 |
Marketing Category | OTC MONOGRAPH NOT FINAL / |
Application Number | part343 |
Labeler Name | Spirit Pharmaceuticals LLC |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient Strength | 500 mg/1; mg/1 |
Pharm Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |