NDC 50844-291

Ibuprofen

Ibuprofen

Ibuprofen is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by L.n.k. International, Inc.. The primary component is Ibuprofen.

Product ID50844-291_1c2b1a49-bb12-4fcc-a9f6-a20e9070f328
NDC50844-291
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 NameL.N.K. International, Inc.
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 50844-291-01

1 BOTTLE, PLASTIC in 1 CARTON (50844-291-01) > 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing Start Date1988-05-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50844-291-01 [50844029101]

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

NDC 50844-291-03 [50844029103]

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

NDC 50844-291-13 [50844029113]

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

NDC 50844-291-14 [50844029114]

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

NDC 50844-291-12 [50844029112]

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

NDC 50844-291-11 [50844029111]

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

NDC 50844-291-08 [50844029108]

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

NDC 50844-291-16 [50844029116]

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

NDC 50844-291-10 [50844029110]

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

NDC 50844-291-02 [50844029102]

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

NDC 50844-291-15 [50844029115]

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

NDC 50844-291-29 [50844029129]

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

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:57b39311-bc20-ace6-75a9-a07a9311b373
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310965
    • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
    • UPC Code
  • 0350844291158
    • 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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