Search by Drug Name or NDC

    NDC 70934-0443-90 Potassium Chloride 750 mg/1 Details

    Potassium Chloride 750 mg/1

    Potassium Chloride is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is POTASSIUM CHLORIDE.

    Product Information

    NDC 70934-0443
    Product ID 70934-443_c8e7ecb2-921a-1197-e053-2a95a90a7ab8
    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 Potassium Chloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Potassium Chloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name POTASSIUM CHLORIDE
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210733
    Listing Certified Through n/a

    Package

    NDC 70934-0443-90 (70934044390)

    NDC Package Code 70934-443-90
    Billing NDC 70934044390
    Package 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-443-90)
    Marketing Start Date 2019-09-16
    NDC Exclude Flag N
    Pricing Information N/A
    << 70934-0442-90 70934-0453-30 >>

    Contents