NDC 62332-213

Amlodipine besylate and Olmesartran medoxomil

Amlodipine Besylate And Olmesartran Medoxomil

Amlodipine besylate and Olmesartran medoxomil is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Alembic Pharmaceuticals Inc.. The primary component is Amlodipine Besylate; Olmesartan Medoxomil.

Product ID62332-213_0cbecf15-09ab-4270-bf17-39693989f36e
NDC62332-213
Product TypeHuman Prescription Drug
Proprietary NameAmlodipine besylate and Olmesartran medoxomil
Generic NameAmlodipine Besylate And Olmesartran Medoxomil
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-07-18
Marketing CategoryANDA / ANDA
Application NumberANDA207073
Labeler NameAlembic Pharmaceuticals Inc.
Substance NameAMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Active Ingredient Strength5 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]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 62332-213-30

30 TABLET, FILM COATED in 1 BOTTLE (62332-213-30)
Marketing Start Date2017-07-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62332-213-90 [62332021390]

Amlodipine besylate and Olmesartran medoxomil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207073
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-07-18

NDC 62332-213-30 [62332021330]

Amlodipine besylate and Olmesartran medoxomil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207073
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-07-18

NDC 62332-213-91 [62332021391]

Amlodipine besylate and Olmesartran medoxomil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207073
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-07-18

Drug Details

Active Ingredients

IngredientStrength
AMLODIPINE BESYLATE5 mg/1

OpenFDA Data

SPL SET ID:1eb78d80-701d-4766-98c3-feee6790de1a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 730872
  • 730861
  • 730866
  • 730869
  • UPC Code
  • 0362332213306
  • 0362332214303
  • 0362332212309
  • 0362332215300
  • Pharmacological Class

    • Calcium Channel Antagonists [MoA]
    • Dihydropyridine Calcium Channel Blocker [EPC]
    • Dihydropyridines [CS]
    • Angiotensin 2 Receptor Antagonists [MoA]
    • Angiotensin 2 Receptor Blocker [EPC]

    Medicade Reported Pricing

    62332021330 AMLODIPINE-OLMESARTAN 5-40 MG

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Amlodipine besylate and Olmesartran medoxomil" or generic name "Amlodipine Besylate And Olmesartran Medoxomil"

    NDCBrand NameGeneric Name
    46708-212Amlodipine besylate and Olmesartran medoxomilAmlodipine besylate and Olmesartran medoxomil
    46708-213Amlodipine besylate and Olmesartran medoxomilAmlodipine besylate and Olmesartran medoxomil
    46708-214Amlodipine besylate and Olmesartran medoxomilAmlodipine besylate and Olmesartran medoxomil
    46708-215Amlodipine besylate and Olmesartran medoxomilAmlodipine besylate and Olmesartran medoxomil
    62332-212Amlodipine besylate and Olmesartran medoxomilAmlodipine besylate and Olmesartran medoxomil
    62332-213Amlodipine besylate and Olmesartran medoxomilAmlodipine besylate and Olmesartran medoxomil
    62332-214Amlodipine besylate and Olmesartran medoxomilAmlodipine besylate and Olmesartran medoxomil
    62332-215Amlodipine besylate and Olmesartran medoxomilAmlodipine besylate and Olmesartran medoxomil

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