NDC 68382-050

meloxicam

Meloxicam

meloxicam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Zydus Pharmaceuticals Usa Inc.. The primary component is Meloxicam.

Product ID68382-050_4a90e955-c151-42b8-aa2d-7e595c7917e7
NDC68382-050
Product TypeHuman Prescription Drug
Proprietary Namemeloxicam
Generic NameMeloxicam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2006-07-19
Marketing CategoryANDA / ANDA
Application NumberANDA077921
Labeler NameZydus Pharmaceuticals USA Inc.
Substance NameMELOXICAM
Active Ingredient Strength8 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 68382-050-01

100 TABLET in 1 BOTTLE (68382-050-01)
Marketing Start Date2006-07-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68382-050-31 [68382005031]

meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-07-19
Marketing End Date2018-02-05

NDC 68382-050-05 [68382005005]

meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077921
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-07-19

NDC 68382-050-77 [68382005077]

meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-07-19

NDC 68382-050-30 [68382005030]

meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-13

NDC 68382-050-40 [68382005040]

meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-07-19

NDC 68382-050-01 [68382005001]

meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077921
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-07-19

NDC 68382-050-16 [68382005016]

meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077921
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-07-19

Drug Details

Active Ingredients

IngredientStrength
MELOXICAM7.5 mg/1

OpenFDA Data

SPL SET ID:6c015f72-5ce3-4f56-8237-776fc2165b0c
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]
    • Anti-Inflammatory Agents
    • Non-Steroidal [CS]

    Medicade Reported Pricing

    68382050206 OMEPRAZOLE-BICARB 40-1,100 CAP

    Pricing Unit: EA | Drug Type:

    68382050106 OMEPRAZOLE-BICARB 20-1,100 CAP

    Pricing Unit: EA | Drug Type:

    68382050010 OMEPRAZOLE DR 40 MG CAPSULE

    Pricing Unit: EA | Drug Type:

    68382050006 OMEPRAZOLE DR 40 MG CAPSULE

    Pricing Unit: EA | Drug Type:

    68382050001 OMEPRAZOLE DR 40 MG CAPSULE

    Pricing Unit: EA | Drug Type:

    68382005005 MELOXICAM 7.5 MG TABLET

    Pricing Unit: EA | Drug Type:

    68382005001 MELOXICAM 7.5 MG TABLET

    Pricing Unit: EA | Drug Type:

    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.