NDC 46708-213

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 Limited. The primary component is Amlodipine Besylate; Olmesartan Medoxomil.

Product ID46708-213_a1a8dc29-8581-4c8f-a1da-1f36587796a7
NDC46708-213
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 Limited
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 Through2020-12-31

Packaging

NDC 46708-213-30

30 TABLET, FILM COATED in 1 BOTTLE (46708-213-30)
Marketing Start Date2017-07-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 46708-213-30 [46708021330]

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

NDC 46708-213-91 [46708021391]

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

NDC 46708-213-90 [46708021390]

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:cb2df7f7-fee8-42ba-8936-0788c4fcc0cb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 730872
  • 730861
  • 730866
  • 730869
  • UPC Code
  • 0346708214302
  • 0346708215309
  • 0346708213305
  • 0346708212308
  • Pharmacological Class

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

    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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