Tylenol PM is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Select Corporation. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.
Product ID | 52904-945_786973d9-0cfa-4a49-97ea-10dab5ac0cec |
NDC | 52904-945 |
Product Type | Human Otc Drug |
Proprietary Name | Tylenol PM |
Generic Name | Acetaminophen And Diphenhydramine Hydrochloride |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 1997-03-01 |
Marketing Category | OTC MONOGRAPH NOT FINAL / |
Application Number | part343 |
Labeler Name | Select Corporation |
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 |
Marketing Start Date | 1997-03-01 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
50269-608 | Tylenol PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
50580-608 | Tylenol PM | acetaminophen and diphenhydramine hydrochloride |
50580-833 | TYLENOL PM | Acetaminophen and Diphenhydramine Hydrochloride |
67751-168 | Tylenol PM | Tylenol PM |
73097-013 | Tylenol PM | Tylenol PM |
0536-1003 | ACETA-GESIC | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
30142-193 | Acetaminophen and Diphenhydramine hydrochloride | Acetaminophen and Diphenhydramine hydrochloride |
49035-026 | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE |
52204-124 | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
37012-771 | Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
41163-515 | Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
30142-755 | Extra Strength Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
21130-095 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
36800-095 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
36800-771 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
37808-795 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
41250-195 | pain relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
49738-783 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
50804-825 | Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
15127-033 | Pain Reliever PM | Acetaminophen and Diphenhydramine Hydrochloride |
0031-8770 | Robitussin Honey Severe Cough, Flu Plus Sore Throat Nighttime | acetaminophen and diphenhydramine hydrochloride |
50405-007 | SohMed Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride |
49483-356 | TIME-GESIC | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
41167-0040 | Unisom PM Pain Nighttime Sleep Aid and Pain Reliever | Acetaminophen and Diphenhydramine Hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TYLENOL PM 74143985 1777613 Live/Registered |
JOHNSON & JOHNSON 1991-03-04 |