Tylenol PM is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Navajo Manufacturing Company Inc.. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.
Product ID | 67751-168_3d1f84be-fde9-1789-e054-00144ff88e88 |
NDC | 67751-168 |
Product Type | Human Otc Drug |
Proprietary Name | Tylenol PM |
Generic Name | Acetaminophen, Diphenhydramine Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2016-09-22 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part343 |
Labeler Name | Navajo Manufacturing Company Inc. |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient Strength | 500 mg/1; mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2016-09-22 |
Marketing End Date | 2021-05-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-09-22 |
Marketing End Date | 2021-05-01 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-09-22 |
Marketing End Date | 2021-05-01 |
Ingredient | Strength |
---|---|
ACETAMINOPHEN | 500 mg/1 |
SPL SET ID: | a729cb7c-2845-4f37-85a1-97e459686e4d |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
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 |
52904-945 | Tylenol PM | acetaminophen and diphenhydramine hydrochloride |
67414-608 | Tylenol PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
67751-168 | Tylenol PM | Tylenol PM |
73097-013 | Tylenol PM | Tylenol PM |
0536-1173 | Acetaminophen, Diphenhydramine Hydrochloride | Acetaminophen, Diphenhydramine Hydrochloride |
0904-6731 | Acetaminophen, Diphenhydramine Hydrochloride | Acetaminophen, Diphenhydramine Hydrochloride |
58602-216 | Aurophen Pain Away plus Sleep aid | acetaminophen, diphenhydramine hydrochloride |
58602-217 | Aurophen Pain Away plus Sleep aid | acetaminophen, diphenhydramine hydrochloride |
62011-0024 | Extra Strength Acetaminophen PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
0904-7651 | Extra Strength Mapap PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
59726-360 | Extra Strength Pain Relief PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
0363-8590 | NightTime Pain Reliever PM | acetaminophen, diphenhydramine hydrochloride |
10202-946 | Pain Away plus Sleep aid | acetaminophen, diphenhydramine hydrochloride |
46122-358 | Pain Plus Sleep | acetaminophen, diphenhydramine hydrochloride |
55910-996 | Pain Relief plus Sleep Aid | acetaminophen, diphenhydramine hydrochloride |
53943-028 | Pain Relief PM | acetaminophen, diphenhydramine hydrochloride |
55319-998 | Pain Relief PM | acetaminophen, diphenhydramine hydrochloride |
59779-905 | Pain Relief PM | acetaminophen, diphenhydramine hydrochloride |
54257-278 | Pain Reliever PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TYLENOL PM 74143985 1777613 Live/Registered |
JOHNSON & JOHNSON 1991-03-04 |