NDC 51645-709
Plus Pharma Extra Strength Acetaminophen PM
Acetaminophen,diphenhydramine Hcl
Plus Pharma Extra Strength Acetaminophen PM is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Gemini Pharmaceuticals, Inc. Dba Plus Pharma. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.
Product ID | 51645-709_994fb1ab-d6e7-610f-e053-2a95a90a25c3 |
NDC | 51645-709 |
Product Type | Human Otc Drug |
Proprietary Name | Plus Pharma Extra Strength Acetaminophen PM |
Generic Name | Acetaminophen,diphenhydramine Hcl |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2006-03-27 |
Marketing End Date | 2021-06-30 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part343 |
Labeler Name | Gemini Pharmaceuticals, Inc. dba Plus Pharma |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient Strength | 500 mg/1; mg/1 |
NDC Exclude Flag | N |