NDC 68788-9990

Etodolac

Etodolac

Etodolac is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is Etodolac.

Product ID68788-9990_24e44ef2-068c-45ea-af89-00623ce991ed
NDC68788-9990
Product TypeHuman Prescription Drug
Proprietary NameEtodolac
Generic NameEtodolac
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2015-04-20
Marketing CategoryANDA / ANDA
Application NumberANDA074903
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameETODOLAC
Active Ingredient Strength500 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-9990-9

90 TABLET, COATED in 1 BOTTLE (68788-9990-9)
Marketing Start Date2015-04-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9990-9 [68788999009]

Etodolac TABLET, COATED
Marketing CategoryANDA
Application NumberANDA074903
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-04-20
Marketing End Date2019-09-16

NDC 68788-9990-3 [68788999003]

Etodolac TABLET, COATED
Marketing CategoryANDA
Application NumberANDA074903
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-04-20
Marketing End Date2019-09-16

NDC 68788-9990-2 [68788999002]

Etodolac TABLET, COATED
Marketing CategoryANDA
Application NumberANDA074903
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-04-20
Marketing End Date2019-09-16

NDC 68788-9990-6 [68788999006]

Etodolac TABLET, COATED
Marketing CategoryANDA
Application NumberANDA074903
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-04-20
Marketing End Date2019-09-16

NDC 68788-9990-8 [68788999008]

Etodolac TABLET, COATED
Marketing CategoryANDA
Application NumberANDA074903
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-04-20
Marketing End Date2019-09-16

NDC 68788-9990-1 [68788999001]

Etodolac TABLET, COATED
Marketing CategoryANDA
Application NumberANDA074903
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-04-20
Marketing End Date2019-09-16

Drug Details

Active Ingredients

IngredientStrength
ETODOLAC500 mg/1

OpenFDA Data

SPL SET ID:d355ce4d-a5d7-4d95-83be-823b1a2a1f98
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199390
    • 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 "Etodolac" or generic name "Etodolac"

    NDCBrand NameGeneric Name
    0093-0892EtodolacEtodolac
    0093-1118EtodolacEtodolac
    0093-1122EtodolacEtodolac
    0093-1893EtodolacEtodolac
    0093-7172EtodolacEtodolac
    0185-0675EtodolacEtodolac
    0185-0687EtodolacEtodolac
    10544-862EtodolacEtodolac
    16714-497EtodolacEtodolac
    16714-498EtodolacEtodolac
    16714-499EtodolacEtodolac
    21695-049EtodolacEtodolac
    21695-050EtodolacEtodolac
    33261-043EtodolacEtodolac
    33261-044EtodolacEtodolac
    35356-324EtodolacEtodolac
    35356-711EtodolacEtodolac
    35356-826EtodolacEtodolac
    42254-052EtodolacEtodolac
    42254-121Etodolacetodolac
    42291-404EtodolacEtodolac
    42291-405EtodolacEtodolac
    42799-111EtodolacEtodolac
    68151-0738EtodolacEtodolac
    68382-273EtodolacEtodolac
    68382-271EtodolacEtodolac
    68382-272EtodolacEtodolac
    68788-6901EtodolacEtodolac
    68788-9410EtodolacEtodolac
    68788-7315EtodolacEtodolac
    68788-7300EtodolacEtodolac
    68788-7068EtodolacEtodolac
    68788-9928EtodolacEtodolac
    68788-9929EtodolacEtodolac
    68788-9360EtodolacEtodolac
    68788-9990EtodolacEtodolac
    68788-9930EtodolacEtodolac
    69238-1342EtodolacEtodolac
    69238-1343EtodolacEtodolac
    70332-320EtodolacEtodolac
    71335-0092EtodolacEtodolac
    71335-0183EtodolacEtodolac
    71335-0399EtodolacEtodolac
    71335-0602EtodolacEtodolac
    71335-0640EtodolacEtodolac
    71335-0126EtodolacEtodolac
    71335-0982EtodolacEtodolac
    43063-578EtodolacEtodolac
    42799-112EtodolacEtodolac
    43063-671EtodolacEtodolac
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.