Percogesic Original Strength is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Medtech Products Inc.. The primary component is Acetaminophen; Diphenhydramine.
| Product ID | 63029-050_d89d64f1-0b97-46d8-96f1-516792498a32 |
| NDC | 63029-050 |
| Product Type | Human Otc Drug |
| Proprietary Name | Percogesic Original Strength |
| Generic Name | Acetaminophen And Diphenhydramine |
| Dosage Form | Tablet, Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-03-19 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Labeler Name | Medtech Products Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE |
| Active Ingredient Strength | 325 mg/1; mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2010-03-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-03-19 |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-03-19 |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-03-19 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 325 mg/1 |
| SPL SET ID: | 85f0a6c8-30c8-4a1f-ac35-542c77a6522a |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 63029-050 | Percogesic Original Strength | Acetaminophen and Diphenhydramine |
| 54473-304 | CounterAct | Acetaminophen and Diphenhydramine |
| 59779-577 | CVS | Acetaminophen and Diphenhydramine |
| 63029-049 | Percogesic Extra Strength | Acetaminophen and Diphenhydramine |