Search by Drug Name or NDC

    NDC 00713-0870-30 Azor 5; 20 mg/1; mg/1 Details

    Azor 5; 20 mg/1; mg/1

    Azor is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cosette Pharmaceuticals, Inc.. The primary component is AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL.

    Product Information

    NDC 00713-0870
    Product ID 0713-0870_00491aef-cf0c-eeb3-e063-6394a90a716d
    Associated GPIs 36993002050310
    GCN Sequence Number 063179
    GCN Sequence Number Description amlodipine bes/olmesartan med TABLET 5 MG-20 MG ORAL
    HIC3 A4H
    HIC3 Description ANGIOTENSIN RECEPTOR BLOCKR-CALCIUM CHANNEL BLOCKR
    GCN 98936
    HICL Sequence Number 035042
    HICL Sequence Number Description AMLODIPINE BESYLATE/OLMESARTAN MEDOXOMIL
    Brand/Generic Brand
    Proprietary Name Azor
    Proprietary Name Suffix n/a
    Non-Proprietary Name amlodipine besylate and olmesartan medoxomil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5; 20
    Active Ingredient Units mg/1; mg/1
    Substance Name AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
    Labeler Name Cosette Pharmaceuticals, Inc.
    Pharmaceutical Class Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA022100
    Listing Certified Through 2024-12-31

    Package

    NDC 00713-0870-30 (00713087030)

    NDC Package Code 0713-0870-30
    Billing NDC 00713087030
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0713-0870-30)
    Marketing Start Date 2022-09-01
    NDC Exclude Flag N
    Pricing Information N/A