NDC 21130-921

Ibuprofen

Ibuprofen

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

Product ID21130-921_18fad17b-c344-453c-a5e9-ef5fbe0db931
NDC21130-921
Product TypeHuman Otc Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1988-05-24
Marketing CategoryANDA / ANDA
Application NumberANDA075010
Labeler NameBetter Living Brands, LLC
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
Pharm ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 21130-921-03

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21130-921-03)
Marketing Start Date1988-05-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 21130-921-14 [21130092114]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24
Marketing End Date2017-05-14

NDC 21130-921-13 [21130092113]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24
Marketing End Date2017-05-14

NDC 21130-921-12 [21130092112]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24
Marketing End Date2017-05-14

NDC 21130-921-03 [21130092103]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 21130-921-15 [21130092115]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24

NDC 21130-921-08 [21130092108]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075010
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-05-24
Marketing End Date2017-05-14

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:73fd99c4-0265-4ae7-88f9-9a22dfdaae04
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310965
    • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
    • UPC Code
  • 0321130777427
    • 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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