NDC 70518-0005

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 ID70518-0005_800d7505-5f85-b430-e053-2991aa0a019e
NDC70518-0005
Product TypeHuman Prescription Drug
Proprietary NameIBUPROFEN
Generic NameIbuprofen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2016-11-17
Marketing CategoryANDA / ANDA
Application NumberANDA090796
Labeler NameREMEDYREPACK INC.
Substance NameIBUPROFEN
Active Ingredient Strength800 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70518-0005-4

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0005-4)
Marketing Start Date2017-02-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-0005-5 [70518000505]

IBUPROFEN TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-05-04
Marketing End Date2019-06-28

NDC 70518-0005-3 [70518000503]

IBUPROFEN TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-27
Marketing End Date2019-06-11

NDC 70518-0005-4 [70518000504]

IBUPROFEN TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-02-06
Marketing End Date2019-07-12

NDC 70518-0005-0 [70518000500]

IBUPROFEN TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-17
Marketing End Date2019-06-04

NDC 70518-0005-2 [70518000502]

IBUPROFEN TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-13
Marketing End Date2019-05-11

NDC 70518-0005-1 [70518000501]

IBUPROFEN TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-05
Marketing End Date2019-06-01

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN800 mg/1

OpenFDA Data

SPL SET ID:9dfc752f-3f66-4c39-bfa8-db6de9a9a9bf
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197807
    • 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]
    • Anti-Inflammatory Agents
    • Non-Steroidal [CS]

    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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