NDC 41163-198

Ibuprofen

Ibuprofen

Ibuprofen is a Oral Capsule, Liquid Filled in the Human Otc Drug category. It is labeled and distributed by Equaline (supervalu). The primary component is Ibuprofen.

Product ID41163-198_093e52ec-9907-464b-9fc5-ddc2df049836
NDC41163-198
Product TypeHuman Otc Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormCapsule, Liquid Filled
Route of AdministrationORAL
Marketing Start Date2012-01-10
Marketing End Date2021-12-30
Marketing CategoryANDA / ANDA
Application NumberANDA078682
Labeler NameEQUALINE (SuperValu)
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN

Packaging

NDC 41163-198-06

160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (41163-198-06)
Marketing Start Date2012-01-10
Marketing End Date2021-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 41163-198-06 [41163019806]

Ibuprofen CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA078682
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-01-10
Marketing End Date2021-12-30

NDC 41163-198-30 [41163019830]

Ibuprofen CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA078682
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-01-10
Marketing End Date2021-12-30

NDC 41163-198-20 [41163019820]

Ibuprofen CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA078682
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-01-10
Marketing End Date2021-12-30

NDC 41163-198-40 [41163019840]

Ibuprofen CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA078682
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-01-10
Marketing End Date2021-12-30

NDC 41163-198-80 [41163019880]

Ibuprofen CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA078682
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-01-10
Marketing End Date2021-12-30

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:c361dec5-67d8-4e1d-94d6-be2f45aaf05a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310964
  • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • NUI Code
  • N0000000160
  • N0000175722
  • N0000175721
  • NDC Crossover Matching brand name "Ibuprofen" or generic name "Ibuprofen"

    NDCBrand NameGeneric Name
    67877-120ibuprofenibuprofen
    67877-119ibuprofenibuprofen
    67877-295ibuprofenibuprofen
    67877-121ibuprofenibuprofen
    67877-294ibuprofenibuprofen
    67877-296ibuprofenibuprofen
    67877-321IbuprofenIbuprofen
    67877-319IbuprofenIbuprofen
    67877-320IbuprofenIbuprofen
    68016-116IbuprofenIbuprofen
    68016-633IbuprofenIbuprofen
    68016-626IbuprofenIbuprofen
    68016-634IbuprofenIbuprofen
    68016-645IbuprofenIbuprofen
    68016-295IbuprofenIbuprofen
    68016-635IbuprofenIbuprofen
    68071-3074IbuprofenIbuprofen
    68071-3362IBUPROFENIBUPROFEN
    68071-4129IbuprofenIbuprofen
    68071-4009IBUPROFENIBUPROFEN
    68071-3388IbuprofenIbuprofen
    68071-4253IbuprofenIbuprofen
    68071-4306IbuprofenIbuprofen
    68071-4357IbuprofenIbuprofen
    68071-4563IbuprofenIbuprofen
    68071-4280IbuprofenIbuprofen
    68071-4243IBUPROFENIBUPROFEN
    68071-4820IbuprofenIbuprofen
    68071-4305IbuprofenIbuprofen
    68071-4459IBUPROFENIBUPROFEN
    68084-703IbuprofenIbuprofen
    68084-658IbuprofenIbuprofen
    68084-772IbuprofenIbuprofen
    68196-980IbuprofenIbuprofen
    68196-981IbuprofenIbuprofen
    68210-0200IBUPROFENIBUPROFEN
    68196-199IbuprofenIbuprofen
    68210-0009IBUPROFENIBUPROFEN
    68196-745IbuprofenIbuprofen
    68387-208IbuprofenIbuprofen
    0472-2002IbuprofenIbuprofen
    68387-210IbuprofenIbuprofen
    68391-121IbuprofenIbuprofen
    68391-199IbuprofenIbuprofen
    0472-1270IbuprofenIbuprofen
    68645-531IbuprofenIbuprofen
    68645-563IbuprofenIbuprofen
    68645-562IbuprofenIbuprofen
    68645-561IbuprofenIbuprofen
    0113-1461basic care childrens ibuprofenIbuprofen

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