NDC 58602-801

Ibuprofen

Ibuprofen

Ibuprofen is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Aurohealth Llc. The primary component is Ibuprofen.

Product ID58602-801_0ade8ee2-7c74-4b05-925e-d92742fc2b90
NDC58602-801
Product TypeHuman Otc Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-11-08
Marketing CategoryANDA / ANDA
Application NumberANDA208865
Labeler NameAurohealth LLC
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58602-801-07

1 BOTTLE in 1 CARTON (58602-801-07) > 24 TABLET in 1 BOTTLE
Marketing Start Date2017-11-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58602-801-88 [58602080188]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-07 [58602080107]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-40 [58602080140]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-87 [58602080187]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-12 [58602080112]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-29 [58602080129]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-36 [58602080136]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-34 [58602080134]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-38 [58602080138]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-15 [58602080115]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-35 [58602080135]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-59 [58602080159]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-14 [58602080114]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-21 [58602080121]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-41 [58602080141]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

NDC 58602-801-19 [58602080119]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA208865
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-08

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:0ade8ee2-7c74-4b05-925e-d92742fc2b90
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310965
    • 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
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