NDC 70771-1374

Exemestane

Exemestane

Exemestane is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Cadila Healthcare Limited. The primary component is Exemestane.

Product ID70771-1374_2301b37f-ea7b-4462-9a2d-196a2e2b042a
NDC70771-1374
Product TypeHuman Prescription Drug
Proprietary NameExemestane
Generic NameExemestane
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-10-08
Marketing CategoryANDA / ANDA
Application NumberANDA202602
Labeler NameCadila Healthcare Limited
Substance NameEXEMESTANE
Active Ingredient Strength25 mg/1
Pharm ClassesAromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70771-1374-3

30 TABLET in 1 BOTTLE (70771-1374-3)
Marketing Start Date2018-10-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70771-1374-3 [70771137403]

Exemestane TABLET
Marketing CategoryANDA
Application NumberANDA202602
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-10-08

Drug Details

Active Ingredients

IngredientStrength
EXEMESTANE25 mg/1

OpenFDA Data

SPL SET ID:fab5468a-d5b7-45e3-b8b2-ed902fddd3a6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310261
  • UPC Code
  • 0370771137435
  • Pharmacological Class

    • Aromatase Inhibitor [EPC]
    • Aromatase Inhibitors [MoA]

    NDC Crossover Matching brand name "Exemestane" or generic name "Exemestane"

    NDCBrand NameGeneric Name
    0054-0080ExemestaneExemestane
    0378-5001Exemestaneexemestane
    0832-0595ExemestaneExemestane
    44278-025ExemestaneEXEMESTANE
    47781-108ExemestaneExemestane
    50090-5193ExemestaneExemestane
    51991-005ExemestaneExemestane
    59651-516ExemestaneExemestane
    59762-2858EXEMESTANEExemestane
    63629-2056ExemestaneExemestane
    65162-240ExemestaneExemestane
    68382-383ExemestaneExemestane
    69097-316EXEMESTANEexemestane
    70771-1374ExemestaneExemestane
    71921-190ExemestaneExemestane
    0009-7663Aromasinexemestane

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