NDC 63256-100

Sclerosol

Talc

Sclerosol is a Intrapleural Aerosol, Powder in the Human Prescription Drug category. It is labeled and distributed by Bryan Corp. The primary component is Talc.

Product ID63256-100_05246011-b7f0-40a3-ac67-b1bd8d23edac
NDC63256-100
Product TypeHuman Prescription Drug
Proprietary NameSclerosol
Generic NameTalc
Dosage FormAerosol, Powder
Route of AdministrationINTRAPLEURAL
Marketing Start Date2013-06-30
Marketing CategoryNDA / NDA
Application NumberNDA020587
Labeler NameBryan Corp
Substance NameTALC
Active Ingredient Strength4 g/25g
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 63256-100-30

1 CANISTER in 1 POUCH (63256-100-30) > 30 g in 1 CANISTER
Marketing Start Date2013-06-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63256-100-30 [63256010030]

Sclerosol AEROSOL, POWDER
Marketing CategoryNDA
Application NumberNDA020587
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2013-06-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
TALC4 g/25g

OpenFDA Data

SPL SET ID:c89eb8fd-6c31-4f8b-8103-1f559424eda1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 546477
  • 546480
  • NDC Crossover Matching brand name "Sclerosol" or generic name "Talc"

    NDCBrand NameGeneric Name
    63256-100SclerosolTalc
    0363-0901BabyTALC
    76271-001DR. WALTONSTALC
    52862-010Health Smart BabyTALC
    43749-112Natures Choice BabyTalc
    50346-004Pan Aromas BabyTALC
    66854-018SPAI-SONSTALC
    63256-200Sterile TalcTalc
    62327-222SteritalcTalc
    62327-333SteritalcTalc
    62327-444SteritalcTalc

    Trademark Results [Sclerosol]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    SCLEROSOL
    SCLEROSOL
    76227242 2515202 Live/Registered
    Bryan Corporation
    2001-03-20

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