Search by Drug Name or NDC

    NDC 70518-3340-00 Promethazine Hydrochloride 25 mg/mL Details

    Promethazine Hydrochloride 25 mg/mL

    Promethazine Hydrochloride is a INTRAMUSCULAR; INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is PROMETHAZINE HYDROCHLORIDE.

    Product Information

    NDC 70518-3340
    Product ID 70518-3340_06cf0b5b-dcae-11fa-e063-6394a90a6aaa
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Promethazine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Promethazine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 25
    Active Ingredient Units mg/mL
    Substance Name PROMETHAZINE HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Phenothiazine [EPC], Phenothiazines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA083312
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3340-00 (70518334000)

    NDC Package Code 70518-3340-0
    Billing NDC 70518334000
    Package 25 AMPULE in 1 CARTON (70518-3340-0) / 1 mL in 1 AMPULE
    Marketing Start Date 2022-01-24
    NDC Exclude Flag N
    Pricing Information N/A