NDC 71105-750

Redicare Ibuprofen

Ibuprofen 200mg

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

Product ID71105-750_45eb33f0-71e3-11d5-e054-00144ff88e88
NDC71105-750
Product TypeHuman Otc Drug
Proprietary NameRedicare Ibuprofen
Generic NameIbuprofen 200mg
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-02-01
Marketing CategoryANDA / ANDA
Application NumberANDA079129
Labeler NameRedicare LLC
Substance NameIBUPROFEN
Active Ingredient Strength200 1/2001
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71105-750-68

1 TABLET, FILM COATED in 1 BOX (71105-750-68)
Marketing Start Date2017-02-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71105-750-68 [71105075068]

Redicare Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA079129
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-02-01

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 1/2001

OpenFDA Data

SPL SET ID:45eb33f0-71e2-11d5-e054-00144ff88e88
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 "Redicare Ibuprofen" or generic name "Ibuprofen 200mg"

    NDCBrand NameGeneric Name
    71105-750Redicare IbuprofenIbuprofen 200mg
    29485-7625IBUPROFENIBUPROFEN 200MG
    29485-9291IBUPROFENIBUPROFEN 200MG
    62959-750IBUPROFENIBUPROFEN 200MG
    67060-001IBUPROFENIBUPROFEN 200MG
    67060-002IBUPROFENIBUPROFEN 200MG
    67060-750IBUPROFENIBUPROFEN 200MG
    53185-381Ibuprofen 200mgIbuprofen 200mg
    69168-382Ibuprofen 200mgIbuprofen 200mg
    69168-390Ibuprofen 200mgIbuprofen 200mg
    69822-693Ibuprofen 200mgIbuprofen 200mg
    0924-0075Physicians Care IbuprofenIbuprofen 200mg
    0924-0076Physicians Care IbuprofenIbuprofen 200mg

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