NDC 0363-1610

IBUPROFEN

Ibuprofen

IBUPROFEN is a Oral Capsule, Liquid Filled in the Human Otc Drug category. It is labeled and distributed by Walgreens. The primary component is Ibuprofen.

Product ID0363-1610_a526d142-965a-5328-e053-2995a90a1d0b
NDC0363-1610
Product TypeHuman Otc Drug
Proprietary NameIBUPROFEN
Generic NameIbuprofen
Dosage FormCapsule, Liquid Filled
Route of AdministrationORAL
Marketing Start Date2016-01-27
Marketing CategoryANDA / ANDA
Application NumberANDA079205
Labeler NameWALGREENS
Substance NameIBUPROFEN
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0363-1610-23

20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-1610-23)
Marketing Start Date2016-01-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-1610-66 [00363161066]

IBUPROFEN CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA079205
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-27
Inactivation Date2020-01-31
Reactivation Date2020-05-08

NDC 0363-1610-23 [00363161023]

IBUPROFEN CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA079205
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-27
Inactivation Date2020-01-31
Reactivation Date2020-05-08

NDC 0363-1610-44 [00363161044]

IBUPROFEN CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA079205
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-27
Inactivation Date2020-01-31
Reactivation Date2020-05-08

NDC 0363-1610-80 [00363161080]

IBUPROFEN CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA079205
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-27
Inactivation Date2020-01-31
Reactivation Date2020-05-08

NDC 0363-1610-31 [00363161031]

IBUPROFEN CAPSULE, LIQUID FILLED
Marketing CategoryANDA
Application NumberANDA079205
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-27
Inactivation Date2020-01-31
Reactivation Date2020-05-08

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

OpenFDA Data

SPL SET ID:3ce5b71b-f841-444f-bf66-023e4bd9aa16
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310964
    • 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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