NDC 51672-4083

Hydrocortisone Butyrate

Hydrocortisone Butyrate

Hydrocortisone Butyrate is a Topical Ointment in the Human Prescription Drug category. It is labeled and distributed by Taro Pharmaceuticals U.s.a., Inc.. The primary component is Hydrocortisone Butyrate.

Product ID51672-4083_26e4c766-6315-4c55-9814-181258a45ad5
NDC51672-4083
Product TypeHuman Prescription Drug
Proprietary NameHydrocortisone Butyrate
Generic NameHydrocortisone Butyrate
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2004-12-27
Marketing CategoryANDA / ANDA
Application NumberANDA076842
Labeler NameTaro Pharmaceuticals U.S.A., Inc.
Substance NameHYDROCORTISONE BUTYRATE
Active Ingredient Strength1 mg/g
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 51672-4083-1

1 TUBE in 1 CARTON (51672-4083-1) > 15 g in 1 TUBE
Marketing Start Date2004-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51672-4083-5 [51672408305]

Hydrocortisone Butyrate OINTMENT
Marketing CategoryANDA
Application NumberANDA076842
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-12-27

NDC 51672-4083-2 [51672408302]

Hydrocortisone Butyrate OINTMENT
Marketing CategoryANDA
Application NumberANDA076842
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-12-27

NDC 51672-4083-1 [51672408301]

Hydrocortisone Butyrate OINTMENT
Marketing CategoryANDA
Application NumberANDA076842
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2004-12-27

NDC 51672-4083-7 [51672408307]

Hydrocortisone Butyrate OINTMENT
Marketing CategoryANDA
Application NumberANDA076842
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-12-27

NDC 51672-4083-6 [51672408306]

Hydrocortisone Butyrate OINTMENT
Marketing CategoryANDA
Application NumberANDA076842
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2004-12-27

Drug Details

Active Ingredients

IngredientStrength
HYDROCORTISONE BUTYRATE1 mg/g

OpenFDA Data

SPL SET ID:51176835-598d-4da7-8a00-6bd36f52aa82
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1370758
  • 1370767
  • 1370770

    • Pharmacological Class

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

    Medicade Reported Pricing

    51672408306 HYDROCORTISONE BUTYR 0.1% OINT

    Pricing Unit: GM | Drug Type:

    51672408301 HYDROCORTISONE BUTYR 0.1% OINT

    Pricing Unit: GM | Drug Type:

    NDC Crossover Matching brand name "Hydrocortisone Butyrate" or generic name "Hydrocortisone Butyrate"

    NDCBrand NameGeneric Name
    0472-0490Hydrocortisone ButyrateHydrocortisone Butyrate
    21695-971Hydrocortisone ButyrateHydrocortisone Butyrate
    51672-4061Hydrocortisone ButyrateHydrocortisone Butyrate
    51672-4074Hydrocortisone ButyrateHydrocortisone Butyrate
    51672-4083Hydrocortisone ButyrateHydrocortisone Butyrate
    51862-159HYDROCORTISONE BUTYRATEHYDROCORTISONE BUTYRATE
    52565-087Hydrocortisone ButyrateHYDROCORTISONE BUTYRATE
    68180-951Hydrocortisone ButyrateHydrocortisone Butyrate
    68462-464Hydrocortisone ButyrateHydrocortisone Butyrate
    68682-270HYDROCORTISONE BUTYRATEHYDROCORTISONE BUTYRATE
    68682-271Hydrocortisone Butyratehydrocortisone butyrate
    68682-273Hydrocortisone Butyratehydrocortisone butyrate
    68682-384Hydrocortisone ButyrateHYDROCORTISONE BUTYRATE
    68682-392HYDROCORTISONE BUTYRATEHYDROCORTISONE BUTYRATE
    68788-7719Hydrocortisone ButyrateHydrocortisone Butyrate Lotion
    70512-032Hydrocortisone ButyrateHydrocortisone Butyrate
    16781-382LocoidHYDROCORTISONE BUTYRATE
    16781-391LocoidHYDROCORTISONE BUTYRATE
    16781-392LocoidHYDROCORTISONE BUTYRATE
    16781-384Locoid LipocreamHYDROCORTISONE BUTYRATE
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