Acetaminophen PM is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Aaa Pharmaceutical, Inc.. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.
Product ID | 57344-095_052c52a3-1bc5-499c-8cc8-b28c1547bd7d |
NDC | 57344-095 |
Product Type | Human Otc Drug |
Proprietary Name | Acetaminophen PM |
Generic Name | Acetaminophen And Diphenhydramine Hydrochloride |
Dosage Form | Tablet, Coated |
Route of Administration | ORAL |
Marketing Start Date | 2012-12-13 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part338 |
Labeler Name | AAA Pharmaceutical, Inc. |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient Strength | 500 mg/1; mg/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2017-07-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-10-01 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-10-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-07-01 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-10-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-10-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-10-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-10-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2012-10-01 |
Marketing End Date | 2019-09-11 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-11-01 |
Ingredient | Strength |
---|---|
ACETAMINOPHEN | 500 mg/1 |
SPL SET ID: | 409b5fcd-5880-4dda-85d8-26aeceb4f8ab |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
11673-556 | Acetaminophen PM | Acetaminophen, Diphenhydramine HCl |
11822-0556 | Acetaminophen PM | Acetaminophen and Diphenhydramine HCl |
17714-133 | ACETAMINOPHEN PM | ACETAMINOPHEN PM |
21130-360 | Acetaminophen PM | Acetaminophen, Diphenhydramine HCl |
30142-530 | acetaminophen pm | Acetaminophen, Diphenhydramine HCl |
30142-700 | acetaminophen pm | Acetaminophen, Diphenhydramine HCl |
30142-800 | acetaminophen pm | Acetaminophen, Diphenhydramine HCl |
37012-771 | Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
41163-228 | Acetaminophen PM | Acetaminophen, Diphenhydramine HCl |
41163-515 | Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride |
41163-956 | Acetaminophen PM | Acetaminophen, Diphenhydramine HCl |
69842-758 | Acetaminophen PM | Acetaminophen PM |
42912-0154 | Acetaminophen PM | Acetaminophen PM |
57344-095 | Acetaminophen PM | Acetaminophen PM |
67510-0154 | Acetaminophen PM | Acetaminophen PM |
73057-352 | ACETAMINOPHEN PM | ACETAMINOPHEN PM |
72036-171 | Acetaminophen PM | Acetaminophen PM |
0536-1003 | ACETA-GESIC | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
30142-193 | Acetaminophen and Diphenhydramine hydrochloride | 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 |
15127-033 | Pain Reliever PM | Acetaminophen and Diphenhydramine Hydrochloride |
0031-8770 | Robitussin Honey Severe Cough, Flu Plus Sore Throat Nighttime | acetaminophen and diphenhydramine hydrochloride |
41167-0040 | Unisom PM Pain Nighttime Sleep Aid and Pain Reliever | Acetaminophen and Diphenhydramine Hydrochloride |