NDC 70518-0761

Ibuprofen

Ibuprofen

Ibuprofen is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Ibuprofen.

Product ID70518-0761_7617c5ad-f7fe-8ece-e053-2991aa0ad8b2
NDC70518-0761
Product TypeHuman Prescription Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-10-06
Marketing CategoryANDA / ANDA
Application NumberANDA091625
Labeler NameREMEDYREPACK INC.
Substance NameIBUPROFEN
Active Ingredient Strength600 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 70518-0761-0

20 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-0)
Marketing Start Date2017-10-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-0761-1 [70518076101]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091625
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-06

NDC 70518-0761-5 [70518076105]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091625
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-09-17

NDC 70518-0761-3 [70518076103]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091625
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-27

NDC 70518-0761-6 [70518076106]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091625
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-07-09

NDC 70518-0761-0 [70518076100]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091625
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-06

NDC 70518-0761-2 [70518076102]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091625
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-26

NDC 70518-0761-4 [70518076104]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091625
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-30

NDC 70518-0761-7 [70518076107]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091625
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-10-16

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN600 mg/1

OpenFDA Data

SPL SET ID:1e6f3ce7-e8a3-40e8-8437-523ef5277b2e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197806
  • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • NUI Code
  • N0000000160
  • N0000175722
  • N0000175721
  • Pharmacological Class

    • Cyclooxygenase Inhibitors [MoA]
    • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
    • Nonsteroidal Anti-inflammatory Drug [EPC]

    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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