ADVIL PM is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Wyeth Consumer Healthcare Llc. The primary component is Diphenhydramine Citrate; Ibuprofen.
Product ID | 0573-0164_11aae8eb-fa5a-4645-96eb-fa9f24e39535 |
NDC | 0573-0164 |
Product Type | Human Otc Drug |
Proprietary Name | ADVIL PM |
Generic Name | Diphenhydramine Citrate And Ibuprofen |
Dosage Form | Tablet, Coated |
Route of Administration | ORAL |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA / NDA |
Application Number | NDA021394 |
Labeler Name | Wyeth Consumer Healthcare LLC |
Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
Active Ingredient Strength | 38 mg/1; mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2005-12-21 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-09-14 |
Marketing End Date | 2018-09-14 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-03-17 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-03-17 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-09-30 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-12-21 |
Marketing Category | NDA |
Application Number | NDA021394 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-12-21 |
Ingredient | Strength |
---|---|
DIPHENHYDRAMINE CITRATE | 38 mg/1 |
SPL SET ID: | 7586892a-32c2-a43f-e053-2991aa0a4680 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
PHarm Class EPC | |
UPC Code | |
NUI Code |
NDC | Brand Name | Generic Name |
---|---|---|
0573-0164 | ADVIL PM | diphenhydramine citrate and ibuprofen |
0573-0167 | ADVIL PM | diphenhydramine HCl, ibuprofen |
66715-9733 | Advil PM | Ibuprofen and Diphenhydramine citrate |
67751-147 | Advil PM | DIPHENHYDRAMINE CITRATE, IBUPROFEN |
29485-6644 | ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated | Advil PM |
29485-7008 | ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated | Advil PM |
29485-7088 | ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated | Advil PM |
29485-7937 | ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coated | Advil PM |
41520-050 | Care One Ibuprofen PM | diphenhydramine citrate and ibuprofen |
55910-050 | dg health Ibuprofen pm | diphenhydramine citrate and ibuprofen |
30142-050 | ibuprofen pm | diphenhydramine citrate and ibuprofen |
59779-050 | ibuprofen pm | diphenhydramine citrate and ibuprofen |
49348-873 | sunmark ibuprofen pm | diphenhydramine citrate and ibuprofen |
36800-050 | Topcare Ibuprofen PM | diphenhydramine citrate and ibuprofen |
11673-050 | up and up ibuprofen pm | diphenhydramine citrate and ibuprofen |