NDC 63629-4108

Diclofenac Potassium

Diclofenac Potassium

Diclofenac Potassium 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 Diclofenac Potassium.

Product ID63629-4108_717341fc-e067-0005-215c-053f6d12e0d1
NDC63629-4108
Product TypeHuman Prescription Drug
Proprietary NameDiclofenac Potassium
Generic NameDiclofenac Potassium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1998-08-11
Marketing CategoryANDA / ANDA
Application NumberANDA075219
Labeler NameBryant Ranch Prepack
Substance NameDICLOFENAC POTASSIUM
Active Ingredient Strength50 mg/1
Pharm ClassesCyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63629-4108-1

20 TABLET, FILM COATED in 1 BOTTLE (63629-4108-1)
Marketing Start Date2009-12-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-4108-3 [63629410803]

Diclofenac Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075219
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-02
Inactivation Date2020-01-31

NDC 63629-4108-6 [63629410806]

Diclofenac Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075219
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-02
Inactivation Date2020-01-31

NDC 63629-4108-8 [63629410808]

Diclofenac Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075219
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-02
Inactivation Date2020-01-31

NDC 63629-4108-7 [63629410807]

Diclofenac Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075219
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-02
Inactivation Date2020-01-31

NDC 63629-4108-5 [63629410805]

Diclofenac Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075219
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-02
Inactivation Date2020-01-31

NDC 63629-4108-2 [63629410802]

Diclofenac Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075219
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-02
Inactivation Date2020-01-31

NDC 63629-4108-4 [63629410804]

Diclofenac Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075219
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-02
Inactivation Date2020-01-31

NDC 63629-4108-1 [63629410801]

Diclofenac Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075219
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-02
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DICLOFENAC POTASSIUM50 mg/1

OpenFDA Data

SPL SET ID:717341fc-e067-0005-215c-053f6d12e0d1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 855942

    • Pharmacological Class

    • Cyclooxygenase Inhibitors [MoA]
    • Decreased Prostaglandin Production [PE]
    • Anti-Inflammatory Agents
    • Non-Steroidal [CS]
    • Nonsteroidal Anti-inflammatory Drug [EPC]

    NDC Crossover Matching brand name "Diclofenac Potassium" or generic name "Diclofenac Potassium"

    NDCBrand NameGeneric Name
    0093-0948Diclofenac PotassiumDiclofenac Potassium
    0378-2474Diclofenac Potassiumdiclofenac potassium
    0480-9435Diclofenac potassiumdiclofenac potassium
    0781-5017Diclofenac PotassiumDiclofenac Potassium
    12634-827DICLOFENAC POTASSIUMDICLOFENAC POTASSIUM
    21695-838Diclofenac PotassiumDiclofenac Potassium
    23155-840diclofenac potassiumdiclofenac potassium
    31722-046Diclofenac potassiumDiclofenac potassium
    33261-038Diclofenac PotassiumDiclofenac Potassium
    35356-713Diclofenac PotassiumDiclofenac Potassium
    43063-848Diclofenac PotassiumDiclofenac Potassium
    49884-905Diclofenac PotassiumDiclofenac Potassium
    50090-0646Diclofenac PotassiumDiclofenac Potassium
    50090-0647Diclofenac PotassiumDiclofenac Potassium
    50090-1535Diclofenac Potassiumdiclofenac potassium
    50090-5893Diclofenac Potassiumdiclofenac potassium
    68071-4042Diclofenac PotassiumDiclofenac Potassium
    68151-0561Diclofenac PotassiumDiclofenac Potassium
    71335-0369Diclofenac PotassiumDiclofenac Potassium
    52959-659Diclofenac PotassiumDiclofenac Potassium
    53002-1176Diclofenac PotassiumDiclofenac Potassium
    55289-781Diclofenac PotassiumDiclofenac Potassium
    61919-072DICLOFENAC POTASSIUMDICLOFENAC POTASSIUM
    63629-4108Diclofenac PotassiumDiclofenac Potassium
    66267-070Diclofenac PotassiumDiclofenac Potassium
    67296-1316Diclofenac PotassiumDiclofenac Potassium
    63629-7969Diclofenac PotassiumDiclofenac Potassium
    70518-2185Diclofenac PotassiumDiclofenac Potassium
    67296-1746Diclofenac PotassiumDiclofenac Potassium
    72789-051Diclofenac PotassiumDiclofenac Potassium
    69292-550Diclofenac PotassiumDiclofenac Potassium
    13913-011Cambiadiclofenac potassium
    13913-012Cambiadiclofenac potassium
    50192-113CAMBIADiclofenac Potassium
    15370-180LOFENADICLOFENAC POTASSIUM
    13913-008ZIPSORdiclofenac potassium
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