NDC 71335-1207

Ibuprofen

Ibuprofen

Ibuprofen is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Ibuprofen.

Product ID71335-1207_0550fa2f-f25e-4abb-b10e-a3d05bdb3217
NDC71335-1207
Product TypeHuman Prescription Drug
Proprietary NameIbuprofen
Generic NameIbuprofen
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2018-08-24
Marketing CategoryANDA / ANDA
Application NumberANDA078329
Labeler NameBryant Ranch Prepack
Substance NameIBUPROFEN
Active Ingredient Strength600 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 71335-1207-0

21 TABLET, FILM COATED in 1 BOTTLE (71335-1207-0)
Marketing Start Date2019-10-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1207-7 [71335120707]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-5 [71335120705]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-6 [71335120706]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-3 [71335120703]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-0 [71335120700]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-4 [71335120704]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-1 [71335120701]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-9 [71335120709]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-8 [71335120708]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

NDC 71335-1207-2 [71335120702]

Ibuprofen TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078329
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-03
Marketing End Date2019-08-07

Drug Details

Active Ingredients

IngredientStrength
IBUPROFEN600 mg/1

OpenFDA Data

SPL SET ID:e8647480-9628-4bcd-a59b-a8f5901fc8d3
Manufacturer
UNII
PHarm Class EPC
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • NUI Code
  • N0000000160
  • N0000175722
  • N0000175721
  • Pharmacological Class

    • Cyclooxygenase Inhibitors [MoA]
    • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
    • Nonsteroidal Anti-inflammatory Drug [EPC]

    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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.