NDC 57896-941

Ibuprofen

Ibuprofen

Ibuprofen is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Geri-care Pharmaceutical Corp. The primary component is Ibuprofen.

Product ID57896-941_61691f99-73d8-e897-e053-2991aa0a3411
NDC57896-941
Product TypeHuman Otc Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2004-01-01
Marketing CategoryANDA / ANDA
Application NumberANDA075010
Labeler NameGeri-Care Pharmaceutical Corp
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 57896-941-01

100 TABLET, FILM COATED in 1 BOTTLE (57896-941-01)
Marketing Start Date2017-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57896-941-10 [57896094110]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-09-01

NDC 57896-941-01 [57896094101]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-09-01

NDC 57896-941-20 [57896094120]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-02-01

NDC 57896-941-25 [57896094125]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-09-01

NDC 57896-941-50 [57896094150]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-09-01

NDC 57896-941-05 [57896094105]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-09-01

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:0744c3ca-4224-4f6a-a033-880949b544fd
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310965
    • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
    • UPC Code
  • 0357896941017
    • 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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