NDC 49348-706

sunmark ibuprofen

Ibuprofen

sunmark ibuprofen is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Strategic Sourcing Services Llc. The primary component is Ibuprofen.

Product ID49348-706_0df15a9c-769d-4a60-839c-af57dfca6d4f
NDC49348-706
Product TypeHuman Otc Drug
Proprietary Namesunmark ibuprofen
Generic NameIbuprofen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2003-06-24
Marketing CategoryANDA / ANDA
Application NumberANDA072096
Labeler NameStrategic Sourcing Services LLC
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 49348-706-04

1 BOTTLE in 1 CARTON (49348-706-04) > 24 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2003-08-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49348-706-14 [49348070614]

sunmark ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072096
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2003-08-21

NDC 49348-706-19 [49348070619]

sunmark ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072096
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2003-08-21
Marketing End Date2012-05-04

NDC 49348-706-09 [49348070609]

sunmark ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072096
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2003-06-24

NDC 49348-706-16 [49348070616]

sunmark ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072096
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-04-12

NDC 49348-706-01 [49348070601]

sunmark ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072096
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-09-28
Marketing End Date2012-10-01

NDC 49348-706-04 [49348070604]

sunmark ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072096
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2003-08-11

NDC 49348-706-42 [49348070642]

sunmark ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072096
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-05-30
Marketing End Date2015-02-04

NDC 49348-706-10 [49348070610]

sunmark ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA072096
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2003-08-11

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:58272a5c-5882-420d-b359-f2c6db836fd2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310965
  • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • NUI Code
  • N0000000160
  • N0000175722
  • N0000175721
  • Medicade Reported Pricing

    49348070616 SM IBUPROFEN 200 MG TABLET

    Pricing Unit: EA | Drug Type:

    49348070614 SM IBUPROFEN 200 MG TABLET

    Pricing Unit: EA | Drug Type:

    49348070610 SM IBUPROFEN 200 MG TABLET

    Pricing Unit: EA | Drug Type:

    49348070609 SM IBUPROFEN 200 MG TABLET

    Pricing Unit: EA | Drug Type:

    49348070604 SM IBUPROFEN 200 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "sunmark ibuprofen" or generic name "Ibuprofen"

    NDCBrand NameGeneric Name
    71335-0746sunmark ibuprofensunmark ibuprofen
    49348-196sunmark ibuprofensunmark ibuprofen
    49348-642sunmark ibuprofensunmark ibuprofen
    49348-229sunmark ibuprofensunmark ibuprofen
    49348-706sunmark ibuprofensunmark ibuprofen
    0113-1461basic care childrens ibuprofenIbuprofen
    0113-7619basic care childrens ibuprofenibuprofen
    0113-7660basic care childrens ibuprofenIbuprofen
    0113-7897Basic Care childrens ibuprofenIbuprofen
    0113-0788Basic Care ibuprofenIbuprofen
    0113-7131basic care ibuprofenIbuprofen
    0113-7517basic care ibuprofenIbuprofen
    0113-7604Basic Care IbuprofenIbuprofen
    0121-0917Childrens IbuprofenIbuprofen
    0121-0914Childrens Ibuprofen Oral SuspensionIbuprofen
    0113-2461Good Sense Childrens IbuprofenIbuprofen
    0113-0057Good Sense ibuprofenibuprofen
    0113-0074Good Sense ibuprofenIbuprofen
    0113-0166good sense ibuprofenIbuprofen
    0113-0298good sense ibuprofenIbuprofen
    0113-0461Good Sense ibuprofenIbuprofen
    0113-0517Good Sense ibuprofenIbuprofen
    0113-0604good sense ibuprofenIbuprofen
    0113-0647good sense ibuprofenIbuprofen
    0113-0660Good Sense IbuprofenIbuprofen
    0113-0685Good Sense IbuprofenIbuprofen
    0113-0897good sense ibuprofenIbuprofen
    0113-1212Good Sense IbuprofenIbuprofen
    0113-4501good sense ibuprofenibuprofen
    0113-0040Good Sense Infants IbuprofenIbuprofen

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.