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    NDC 71205-0982-00 Salsalate 500 mg/1 Details

    Salsalate 500 mg/1

    Salsalate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is SALSALATE.

    Product Information

    NDC 71205-0982
    Product ID 71205-982_9ac60e91-481e-4681-83d6-f0c62114f627
    Associated GPIs 64100075000305
    GCN Sequence Number 004438
    GCN Sequence Number Description salsalate TABLET 500 MG ORAL
    HIC3 H3D
    HIC3 Description ANALGESIC/ANTIPYRETICS, SALICYLATES
    GCN 16801
    HICL Sequence Number 001845
    HICL Sequence Number Description SALSALATE
    Brand/Generic Generic
    Proprietary Name Salsalate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Salsalate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name SALSALATE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0982-00 (71205098200)

    NDC Package Code 71205-982-00
    Billing NDC 71205098200
    Package 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-982-00)
    Marketing Start Date 2020-05-07
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 52021032-7ab6-48e0-b290-994bae0e44cc Details

    Revised: 11/2022