NDC 0573-0164

ADVIL PM

Diphenhydramine Citrate And Ibuprofen

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 ID0573-0164_11aae8eb-fa5a-4645-96eb-fa9f24e39535
NDC0573-0164
Product TypeHuman Otc Drug
Proprietary NameADVIL PM
Generic NameDiphenhydramine Citrate And Ibuprofen
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2005-12-21
Marketing CategoryNDA / NDA
Application NumberNDA021394
Labeler NameWyeth Consumer Healthcare LLC
Substance NameDIPHENHYDRAMINE CITRATE; IBUPROFEN
Active Ingredient Strength38 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0573-0164-04

4 TABLET, COATED in 1 POUCH (0573-0164-04)
Marketing Start Date2005-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0573-0164-45 [00573016445]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-49 [00573016449]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-14 [00573016414]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-12-21

NDC 0573-0164-20 [00573016420]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-12-21

NDC 0573-0164-32 [00573016432]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-34 [00573016434]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-14
Marketing End Date2018-09-14

NDC 0573-0164-05 [00573016405]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-12-21

NDC 0573-0164-04 [00573016404]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-30 [00573016430]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-12-21

NDC 0573-0164-43 [00573016443]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-12-21

NDC 0573-0164-33 [00573016433]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-55 [00573016455]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-12-21

NDC 0573-0164-08 [00573016408]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-03-17

NDC 0573-0164-41 [00573016441]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-09 [00573016409]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-03-17

NDC 0573-0164-44 [00573016444]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-21 [00573016421]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-65 [00573016465]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-09-30

NDC 0573-0164-91 [00573016491]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

NDC 0573-0164-12 [00573016412]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-12-21

NDC 0573-0164-40 [00573016440]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-12-21

NDC 0573-0164-46 [00573016446]

ADVIL PM TABLET, COATED
Marketing CategoryNDA
Application NumberNDA021394
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-12-21

Drug Details

Active Ingredients

IngredientStrength
DIPHENHYDRAMINE CITRATE38 mg/1

OpenFDA Data

SPL SET ID:7586892a-32c2-a43f-e053-2991aa0a4680
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 895664
  • 901818
  • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • UPC Code
  • 0305730164306
  • NUI Code
  • N0000000160
  • N0000175722
  • N0000175721
  • NDC Crossover Matching brand name "ADVIL PM" or generic name "Diphenhydramine Citrate And Ibuprofen"

    NDCBrand NameGeneric Name
    0573-0164ADVIL PMdiphenhydramine citrate and ibuprofen
    0573-0167ADVIL PMdiphenhydramine HCl, ibuprofen
    66715-9733Advil PMIbuprofen and Diphenhydramine citrate
    67751-147Advil PMDIPHENHYDRAMINE CITRATE, IBUPROFEN
    29485-6644ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coatedAdvil PM
    29485-7008ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coatedAdvil PM
    29485-7088ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coatedAdvil PM
    29485-7937ADVIL PM- diphenhydramine citrate and ibuprofen tablet, coatedAdvil PM
    41520-050Care One Ibuprofen PMdiphenhydramine citrate and ibuprofen
    55910-050dg health Ibuprofen pmdiphenhydramine citrate and ibuprofen
    30142-050ibuprofen pmdiphenhydramine citrate and ibuprofen
    59779-050ibuprofen pmdiphenhydramine citrate and ibuprofen
    49348-873sunmark ibuprofen pmdiphenhydramine citrate and ibuprofen
    36800-050Topcare Ibuprofen PMdiphenhydramine citrate and ibuprofen
    11673-050up and up ibuprofen pmdiphenhydramine citrate and ibuprofen

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