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 |