NDC 0006-5374

SEGLUROMET

Ertugliflozin And Metformin Hydrochloride

SEGLUROMET is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Merck Sharp & Dohme Corp.. The primary component is Ertugliflozin Pidolate; Metformin Hydrochloride.

Product ID0006-5374_104d4fc3-1be2-454b-9582-becbd99b3c1a
NDC0006-5374
Product TypeHuman Prescription Drug
Proprietary NameSEGLUROMET
Generic NameErtugliflozin And Metformin Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-12-19
Marketing CategoryNDA / NDA
Application NumberNDA209806
Labeler NameMerck Sharp & Dohme Corp.
Substance NameERTUGLIFLOZIN PIDOLATE; METFORMIN HYDROCHLORIDE
Active Ingredient Strength8 mg/1; mg/1
Pharm ClassesBiguanide [EPC],Biguanides [CS]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0006-5374-03

60 TABLET, FILM COATED in 1 BOTTLE (0006-5374-03)
Marketing Start Date2017-12-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0006-5374-08 [00006537408]

SEGLUROMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA209806
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-19

NDC 0006-5374-09 [00006537409]

SEGLUROMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA209806
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-19

NDC 0006-5374-07 [00006537407]

SEGLUROMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA209806
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-19

NDC 0006-5374-06 [00006537406]

SEGLUROMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA209806
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-19

NDC 0006-5374-03 [00006537403]

SEGLUROMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA209806
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-19

Drug Details

Active Ingredients

IngredientStrength
ERTUGLIFLOZIN PIDOLATE7.5 mg/1

OpenFDA Data

SPL SET ID:a6aeb99a-ce49-4125-90ce-642df3f1ebad
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1992685
  • 1992695
  • 1992693
  • 1992691
  • 1992698
  • 1992701
  • 1992700
  • 1992703
  • UPC Code
  • 0300065374031
  • 0300065373034
  • 0300065370033
  • 0300065369037
  • Pharmacological Class

    • Biguanide [EPC]
    • Biguanides [CS]

    NDC Crossover Matching brand name "SEGLUROMET" or generic name "Ertugliflozin And Metformin Hydrochloride"

    NDCBrand NameGeneric Name
    0006-5369SEGLUROMETertugliflozin and metformin hydrochloride
    0006-5370SEGLUROMETertugliflozin and metformin hydrochloride
    0006-5373SEGLUROMETertugliflozin and metformin hydrochloride
    0006-5374SEGLUROMETertugliflozin and metformin hydrochloride
    50090-6217SEGLUROMETertugliflozin and metformin hydrochloride
    50090-6218SEGLUROMETertugliflozin and metformin hydrochloride
    50090-6231SEGLUROMETertugliflozin and metformin hydrochloride

    Trademark Results [SEGLUROMET]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    SEGLUROMET
    SEGLUROMET
    86727956 5570929 Live/Registered
    Merck Sharp & Dohme Corp.
    2015-08-18

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