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    NDC 51672-2117-04 Feverall 650 mg/1 Details

    Feverall 650 mg/1

    Feverall is a RECTAL SUPPOSITORY in the HUMAN OTC DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A. Inc.. The primary component is ACETAMINOPHEN.

    Product Information

    NDC 51672-2117
    Product ID 51672-2117_c107ee4d-6fd8-4cd8-9f80-5d140801eaba
    Associated GPIs 64200010005220
    GCN Sequence Number 004478
    GCN Sequence Number Description acetaminophen SUPP.RECT 650 MG RECTAL
    HIC3 H3E
    HIC3 Description ANALGESIC/ANTIPYRETICS,NON-SALICYLATE
    GCN 16907
    HICL Sequence Number 001866
    HICL Sequence Number Description ACETAMINOPHEN
    Brand/Generic Brand
    Proprietary Name Feverall
    Proprietary Name Suffix Adults
    Non-Proprietary Name Acetaminophen
    Product Type HUMAN OTC DRUG
    Dosage Form SUPPOSITORY
    Route RECTAL
    Active Ingredient Strength 650
    Active Ingredient Units mg/1
    Substance Name ACETAMINOPHEN
    Labeler Name Taro Pharmaceuticals U.S.A. Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA018337
    Listing Certified Through 2024-12-31

    Package

    NDC 51672-2117-04 (51672211704)

    NDC Package Code 51672-2117-4
    Billing NDC 51672211704
    Package 50 BLISTER PACK in 1 CARTON (51672-2117-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2117-0)
    Marketing Start Date 2013-12-12
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 7afa4b78-5e14-4723-a87b-01f664b0c0e9 Details

    Revised: 5/2016