NDC 51991-005

Exemestane

Exemestane

Exemestane is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Breckenridge Pharmaceutical, Inc.. The primary component is Exemestane.

Product ID51991-005_3f71b752-81ae-4726-8f0a-204dcc9bfeef
NDC51991-005
Product TypeHuman Prescription Drug
Proprietary NameExemestane
Generic NameExemestane
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-12-19
Marketing CategoryANDA / ANDA
Application NumberANDA211031
Labeler NameBreckenridge Pharmaceutical, Inc.
Substance NameEXEMESTANE
Active Ingredient Strength25 mg/1
Pharm ClassesAromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 51991-005-33

30 TABLET, FILM COATED in 1 BOTTLE (51991-005-33)
Marketing Start Date2019-12-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51991-005-33 [51991000533]

Exemestane TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA211031
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-12-19

Drug Details

Active Ingredients

IngredientStrength
EXEMESTANE25 mg/1

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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