NDC 0781-4063

Aprepitant

Aprepitant

Aprepitant is a Kit in the Human Prescription Drug category. It is labeled and distributed by Sandoz Inc. The primary component is .

Product ID0781-4063_6355a06a-3314-4666-adcb-ee10e732c3bc
NDC0781-4063
Product TypeHuman Prescription Drug
Proprietary NameAprepitant
Generic NameAprepitant
Dosage FormKit
Marketing Start Date2016-12-27
Marketing CategoryANDA / ANDA
Application NumberANDA090999
Labeler NameSandoz Inc
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0781-4063-36

1 KIT in 1 DOSE PACK (0781-4063-36) * 2 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACK
Marketing Start Date2016-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0781-4063-36 [00781406336]

Aprepitant KIT
Marketing CategoryANDA
Application NumberANDA090999
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-12-27

Drug Details

OpenFDA Data

SPL SET ID:f58b8944-93ee-4be1-a238-cc0061ddd93a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 644088
  • 403810
  • 403811
  • 754508

    • NDC Crossover Matching brand name "Aprepitant" or generic name "Aprepitant"

    NDCBrand NameGeneric Name
    0781-2321Aprepitantaprepitant
    0781-2322Aprepitantaprepitant
    68462-112AprepitantAprepitant
    68462-583AprepitantAprepitant
    68462-584AprepitantAprepitant
    68462-585AprepitantAprepitant
    0781-2323AprepitantAprepitant
    0781-4063AprepitantAprepitant
    13668-594APREPITANTAPREPITANT
    13668-591APREPITANTAPREPITANT
    13668-592APREPITANTAPREPITANT
    13668-593APREPITANTAPREPITANT
    0006-0461EMENDaprepitant
    0006-0462EMENDaprepitant
    0006-0464EMENDaprepitant
    0006-3066EMENDaprepitant
    0006-3862EMENDaprepitant
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.