NDC 68180-775

Amlodipine, Valsartan and Hydrochlorothiazide

Amlodipine, Valsartan And Hydrochlorothiazide

Amlodipine, Valsartan and Hydrochlorothiazide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is Amlodipine Besylate; Valsartan; Hydrochlorothiazide.

Product ID68180-775_0670fd76-339b-48eb-a77c-e96bb1d75f80
NDC68180-775
Product TypeHuman Prescription Drug
Proprietary NameAmlodipine, Valsartan and Hydrochlorothiazide
Generic NameAmlodipine, Valsartan And Hydrochlorothiazide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2015-06-04
Marketing CategoryANDA / ANDA
Application NumberANDA200797
Labeler NameLupin Pharmaceuticals, Inc.
Substance NameAMLODIPINE BESYLATE; VALSARTAN; HYDROCHLOROTHIAZIDE
Active Ingredient Strength10 mg/1; mg/1; mg/1
Pharm ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 68180-775-02

500 TABLET, FILM COATED in 1 BOTTLE (68180-775-02)
Marketing Start Date2015-06-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68180-775-09 [68180077509]

Amlodipine, Valsartan and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-06-04

NDC 68180-775-02 [68180077502]

Amlodipine, Valsartan and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200797
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-06-04

NDC 68180-775-06 [68180077506]

Amlodipine, Valsartan and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200797
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-06-04

Drug Details

Active Ingredients

IngredientStrength
AMLODIPINE BESYLATE10 mg/1

OpenFDA Data

SPL SET ID:5dbb43b1-3ea4-4fa5-a9aa-95d869ae65fe
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 848151
  • 848145
  • 848131
  • 848140
  • 848135
    • UPC Code
  • 0368180774068
  • 0368180775065
  • 0368180773061
  • 0368180771067

    • Pharmacological Class

    • Calcium Channel Antagonists [MoA]
    • Dihydropyridine Calcium Channel Blocker [EPC]
    • Dihydropyridines [CS]
    • Angiotensin 2 Receptor Antagonists [MoA]
    • Angiotensin 2 Receptor Blocker [EPC]
    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]

    Medicade Reported Pricing

    68180077509 AMLODIPINE-VALSARTAN-HYDROCHLOROTHIAZIDE 10-320-25 MG TAB

    Pricing Unit: EA | Drug Type:

    68180077506 AMLODIPINE-VALSARTAN-HYDROCHLOROTHIAZIDE 10-320-25 MG TAB

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Amlodipine, Valsartan and Hydrochlorothiazide" or generic name "Amlodipine, Valsartan And Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    13668-325Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    13668-326Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    13668-327Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    13668-328Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    13668-329Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    57297-771Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    57297-772Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    57297-773Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    57297-774Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    57297-775Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    65862-834Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    65862-835Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    65862-836Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    65862-837Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    65862-838Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    68180-771Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    68180-772Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    68180-773Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    68180-775Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    68180-774Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
    70518-1220Amlodipine, Valsartan and HydrochlorothiazideAmlodipine, Valsartan and Hydrochlorothiazide
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