High Outlier
Strength
200 mg/1
Manufacturer
Acertis Pharmaceuticals, LLCNDC
72989037330
Classification
Brand
Dosage Form
CAPSULE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
PROGESTERONEApproval Type
New Drug (NDA)
FDA Application
NDA019781On Market Since
11/1/2022
Pharmacological Classes
Progesterone
Progesterone
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