NDC 67046-306

ibuprofen

Ibuprofen

ibuprofen is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Ibuprofen.

Product ID67046-306_5abea399-8ee0-7238-e053-2991aa0ae155
NDC67046-306
Product TypeHuman Prescription Drug
Proprietary Nameibuprofen
Generic NameIbuprofen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-10-04
Marketing CategoryANDA / ANDA
Application NumberANDA090796
Labeler NameContract Pharmacy Services-PA
Substance NameIBUPROFEN
Active Ingredient Strength400 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 67046-306-30

30 TABLET in 1 BLISTER PACK (67046-306-30)
Marketing Start Date2017-10-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-306-60 [67046030660]

ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Inactivation Date2020-01-31

NDC 67046-306-20 [67046030620]

ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Inactivation Date2020-01-31

NDC 67046-306-14 [67046030614]

ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Inactivation Date2020-01-31

NDC 67046-306-28 [67046030628]

ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Inactivation Date2020-01-31

NDC 67046-306-21 [67046030621]

ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Inactivation Date2020-01-31

NDC 67046-306-15 [67046030615]

ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Inactivation Date2020-01-31

NDC 67046-306-30 [67046030630]

ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Inactivation Date2020-01-31

NDC 67046-306-07 [67046030607]

ibuprofen TABLET
Marketing CategoryANDA
Application NumberANDA090796
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-04
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN400 mg/1

OpenFDA Data

SPL SET ID:5abea399-8edf-7238-e053-2991aa0ae155
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197805
    • PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
    • UPC Code
  • 0367877294056
    • NUI Code
  • N0000000160
  • N0000175722
  • N0000175721

    • Pharmacological Class

    • Cyclooxygenase Inhibitors [MoA]
    • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
    • Nonsteroidal Anti-inflammatory Drug [EPC]
    • Anti-Inflammatory Agents
    • Non-Steroidal [CS]

    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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