NDC 0363-0393

Ibuprofen 200

Ibuprofen

Ibuprofen 200 is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Ibuprofen.

Product ID0363-0393_0ee1e059-0dd6-40ad-b586-6e7f05964e73
NDC0363-0393
Product TypeHuman Otc Drug
Proprietary NameIbuprofen 200
Generic NameIbuprofen
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date1999-03-01
Marketing CategoryANDA / ANDA
Application NumberANDA075139
Labeler NameWalgreen Company
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0363-0393-12

1 BOTTLE in 1 CARTON (0363-0393-12) > 100 TABLET, COATED in 1 BOTTLE
Marketing Start Date1999-03-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-0393-37 [00363039337]

Ibuprofen 200 TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-03-01
Marketing End Date2021-02-07

NDC 0363-0393-08 [00363039308]

Ibuprofen 200 TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1999-03-01
Marketing End Date2015-10-15

NDC 0363-0393-15 [00363039315]

Ibuprofen 200 TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1999-03-01

NDC 0363-0393-12 [00363039312]

Ibuprofen 200 TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1999-03-01

NDC 0363-0393-14 [00363039314]

Ibuprofen 200 TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1999-03-01

NDC 0363-0393-20 [00363039320]

Ibuprofen 200 TABLET, COATED
Marketing CategoryANDA
Application NumberANDA075139
Product TypeHUMAN OTC DRUG
Marketing Start Date1999-03-01

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:62e8db95-aaef-4b0e-841e-64a0339f3190
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310965
  • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • UPC Code
  • 0311917177564
  • NUI Code
  • N0000000160
  • N0000175722
  • N0000175721
  • NDC Crossover Matching brand name "Ibuprofen 200" or generic name "Ibuprofen"

    NDCBrand NameGeneric Name
    0363-0393Ibuprofen 200Ibuprofen 200
    0363-0222Ibuprofen 200Ibuprofen 200
    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

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