NDC 63629-2056

Exemestane

Exemestane

Exemestane is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Exemestane.

Product ID63629-2056_1841ec12-3f4f-4b87-b719-fd0b4d9eaffb
NDC63629-2056
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 NameBryant Ranch Prepack
Substance NameEXEMESTANE
Active Ingredient Strength25 mg/1
Pharm ClassesAromatase Inhibitor [EPC], Aromatase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63629-2056-1

30 TABLET, FILM COATED in 1 BOTTLE (63629-2056-1)
Marketing Start Date2019-12-19
NDC Exclude FlagN
Sample Package?N

Drug Details

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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