Extra Strength Acetaminophen PM is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Cardinal Health. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.
| Product ID | 70000-0149_7483340b-6090-4fc4-e053-2991aa0a7503 |
| NDC | 70000-0149 |
| Product Type | Human Otc Drug |
| Proprietary Name | Extra Strength Acetaminophen PM |
| Generic Name | Acetaminophen And Diphenhydramine Hcl |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-11-22 |
| Marketing End Date | 2020-05-31 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part343 |
| Labeler Name | Cardinal Health |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient Strength | 500 mg/1; mg/1 |
| NDC Exclude Flag | N |
| Marketing Start Date | 2016-11-22 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2017-01-25 |
| Marketing End Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-11-22 |
| Marketing End Date | 2020-05-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part343 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-11-22 |
| Marketing End Date | 2020-05-31 |
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 500 mg/1 |
| SPL SET ID: | 41eac1e2-dfa8-2b99-e054-00144ff8d46c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 30142-755 | Extra Strength Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
| 68210-1000 | EXTRA STRENGTH ACETAMINOPHEN PM | EXTRA STRENGTH ACETAMINOPHEN PM |
| 70000-0149 | Extra Strength Acetaminophen PM | Extra Strength Acetaminophen PM |
| 62011-0025 | Extra Strength Acetaminophen PM | Extra Strength Acetaminophen PM |
| 62011-0024 | Extra Strength Acetaminophen PM | Extra Strength Acetaminophen PM |
| 0536-3479 | Acetaminophen and Diphenhydramine HCl | Acetaminophen and Diphenhydramine HCl |
| 49035-235 | Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 55319-235 | Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 55319-556 | Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 37205-759 | Extra Strength Pain Reliever PM | Acetaminophen and Diphenhydramine HCl |
| 49738-999 | KMart - Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 11822-0556 | Pain Relief Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 11822-2350 | Pain Relief Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
| 21130-556 | Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 49738-655 | Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 55910-655 | Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 15127-325 | Pain Reliever PM | Acetaminophen and Diphenhydramine HCl |
| 0135-0608 | PANADOL | acetaminophen and diphenhydramine HCl |
| 0135-7021 | PANADOL | acetaminophen and diphenhydramine HCl |
| 41250-556 | Rapid Release Pain Relief PM | Acetaminophen and Diphenhydramine HCl |
| 0363-0235 | Wal-Nadol PM | Acetaminophen and Diphenhydramine HCl |