NDC 50090-2463

Ibuprofen

Ibuprofen

Ibuprofen is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Ibuprofen.

Product ID50090-2463_47a219a7-ff5e-4a93-b0b3-23c8fcc12272
NDC50090-2463
Product TypeHuman Otc Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-03-01
Marketing CategoryANDA / ANDA
Application NumberANDA091239
Labeler NameA-S Medication Solutions
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 50090-2463-0

50 TABLET in 1 BOTTLE (50090-2463-0)
Marketing Start Date2016-09-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-2463-5 [50090246305]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-10

NDC 50090-2463-2 [50090246302]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-06

NDC 50090-2463-0 [50090246300]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-09-12

NDC 50090-2463-8 [50090246308]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-12-14

NDC 50090-2463-3 [50090246303]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-09-06

NDC 50090-2463-4 [50090246304]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-06

NDC 50090-2463-6 [50090246306]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-01-04

NDC 50090-2463-7 [50090246307]

Ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA091239
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-09-20

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:994cb67c-d77d-4319-a4ee-6c4d239ce6c3
Manufacturer
UNII
PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • 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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