NDC 0168-0280

amcinonide

Amcinonide

amcinonide is a Topical Lotion in the Human Prescription Drug category. It is labeled and distributed by E. Fougera & Co. A Division Of Fougera Pharmaceuticals Inc.. The primary component is Amcinonide.

Product ID0168-0280_34be0cb1-729f-4cd3-98b2-15a4dd48b3bd
NDC0168-0280
Product TypeHuman Prescription Drug
Proprietary Nameamcinonide
Generic NameAmcinonide
Dosage FormLotion
Route of AdministrationTOPICAL
Marketing Start Date2002-11-06
Marketing CategoryANDA / ANDA
Application NumberANDA076329
Labeler NameE. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Substance NameAMCINONIDE
Active Ingredient Strength1 mg/g
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0168-0280-60

1 BOTTLE in 1 CARTON (0168-0280-60) > 60 g in 1 BOTTLE
Marketing Start Date2002-11-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0168-0280-60 [00168028060]

amcinonide LOTION
Marketing CategoryANDA
Application NumberANDA076329
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2002-11-06

Drug Details

Active Ingredients

IngredientStrength
AMCINONIDE1 mg/g

OpenFDA Data

SPL SET ID:cb46264b-7df2-4fb8-ae8d-cfa96570e781
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199041
  • Pharmacological Class

    • Corticosteroid [EPC]
    • Corticosteroid Hormone Receptor Agonists [MoA]
    • Corticosteroid [EPC]
    • Corticosteroid Hormone Receptor Agonists [MoA]

    NDC Crossover Matching brand name "amcinonide" or generic name "Amcinonide"

    NDCBrand NameGeneric Name
    0168-0278AmcinonideAmcinonide
    0168-0279Amcinonideamcinonide
    0168-0280amcinonideamcinonide
    51672-4054AmcinonideAmcinonide
    51672-4060AmcinonideAmcinonide

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