Product Details for: Follistim AQ

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Subcutaneous, Intramuscular
75IU/0.5ML
Single-Dose Vial
351(a)
Follistim AQ
Disc
002
Injection
Subcutaneous, Intramuscular
150IU/0.5ML
Single-Dose Vial
351(a)
Follistim AQ
Disc
Proper Name
follitropin beta
BLA Number
021273
Applicant
Organon USA Inc., a subsidiary of Merck & Co., Inc.
Original Approval Date
August 26, 2005
Date of First Licensure
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