NDC 63629-3328

meloxicam

Meloxicam

meloxicam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Meloxicam.

Product ID63629-3328_68ae5c1f-b624-4cf3-905f-f0f0c092a206
NDC63629-3328
Product TypeHuman Prescription Drug
Proprietary Namemeloxicam
Generic NameMeloxicam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-03-07
Marketing CategoryANDA / ANDA
Application NumberANDA077927
Labeler NameBryant Ranch Prepack
Substance NameMELOXICAM
Active Ingredient Strength15 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 63629-3328-0

20 TABLET in 1 BOTTLE (63629-3328-0)
Marketing Start Date2010-10-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-3328-5 [63629332805]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-1 [63629332801]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-0 [63629332800]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-3 [63629332803]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-9 [63629332809]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-4 [63629332804]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-7 [63629332807]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-6 [63629332806]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-2 [63629332802]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

NDC 63629-3328-8 [63629332808]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-07
Marketing End Date2019-08-18

Drug Details

Active Ingredients

IngredientStrength
MELOXICAM15 mg/1

OpenFDA Data

SPL SET ID:a381942f-0cba-4e97-4741-ad04a6af2164
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 152695
  • 311486
  • 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 "meloxicam" or generic name "Meloxicam"

    NDCBrand NameGeneric Name
    0179-0179meloxicammeloxicam
    0179-0180meloxicammeloxicam
    0440-5841MeloxicamMeloxicam
    0440-6841MeloxicamMeloxicam
    0615-6568MeloxicamMeloxicam
    0615-6569MeloxicamMeloxicam
    0615-7885MeloxicamMeloxicam
    0615-7886meloxicammeloxicam
    0615-8040MELOXICAMmeloxicam
    0615-8124MELOXICAMMeloxicam
    10544-052MeloxicamMeloxicam
    10544-090MeloxicamMeloxicam
    10544-251MeloxicamMeloxicam
    10544-252MeloxicamMeloxicam
    10544-555meloxicammeloxicam
    10544-631meloxicammeloxicam
    10544-925meloxicammeloxicam
    16571-776MeloxicamMeloxicam
    16571-777MeloxicamMeloxicam
    21695-076MeloxicamMeloxicam
    21695-077Meloxicammeloxicam
    29300-124meloxicammeloxicam
    29300-125meloxicammeloxicam
    33261-070meloxicammeloxicam
    33261-071meloxicammeloxicam
    35356-808meloxicammeloxicam
    68071-1919MELOXICAMMELOXICAM
    68071-2184MELOXICAMMELOXICAM
    68071-1994meloxicammeloxicam
    68071-1993meloxicammeloxicam
    68151-4319meloxicammeloxicam
    68180-501MeloxicamMeloxicam
    68180-502MeloxicamMeloxicam
    68382-051meloxicammeloxicam
    68382-050meloxicammeloxicam
    68462-141MeloxicamMeloxicam
    68462-140MeloxicamMeloxicam
    68788-1701meloxicammeloxicam
    68788-9897meloxicammeloxicam
    68788-9418meloxicammeloxicam
    68788-9898meloxicammeloxicam
    69097-159MELOXICAMMELOXICAM
    69097-158MELOXICAMMELOXICAM
    69336-101MeloxicamMeloxicam
    69336-102MeloxicamMeloxicam
    70518-0031meloxicammeloxicam
    70518-0200MELOXICAMMELOXICAM
    70518-0039meloxicammeloxicam
    70518-0394meloxicammeloxicam
    70518-0171MELOXICAMMELOXICAM

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