Search by Drug Name or NDC

    NDC 24689-0137-01 Sodium Bicarbonate 650 mg/1 Details

    Sodium Bicarbonate 650 mg/1

    Sodium Bicarbonate is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by APNAR PHARMA LP. The primary component is SODIUM BICARBONATE.

    Product Information

    NDC 24689-0137
    Product ID 24689-137_08352100-b59d-c799-e063-6294a90a5e3b
    Associated GPIs
    GCN Sequence Number 002661
    GCN Sequence Number Description sodium bicarbonate TABLET 650 MG ORAL
    HIC3 D4B
    HIC3 Description ANTACIDS
    GCN 07855
    HICL Sequence Number 000523
    HICL Sequence Number Description SODIUM BICARBONATE
    Brand/Generic Generic
    Proprietary Name Sodium Bicarbonate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sodium Bicarbonate
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 650
    Active Ingredient Units mg/1
    Substance Name SODIUM BICARBONATE
    Labeler Name APNAR PHARMA LP
    Pharmaceutical Class Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M001
    Listing Certified Through 2024-12-31

    Package

    NDC 24689-0137-01 (24689013701)

    NDC Package Code 24689-137-01
    Billing NDC 24689013701
    Package 1000 TABLET in 1 BOTTLE (24689-137-01)
    Marketing Start Date 2022-06-24
    NDC Exclude Flag N
    Pricing Information N/A