Progesterone
Progesterone Capsules 100 mg and 200 mg
Approved
Approval ID
1c71a4b0-1347-498f-8124-f4cb4be27b61
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 9, 2022
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Progesterone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71335-1443
Application NumberANDA211285
Product Classification
M
Marketing Category
C73584
G
Generic Name
Progesterone
Product Specifications
Route of AdministrationORAL
Effective DateMay 20, 2021
FDA Product Classification
INGREDIENTS (9)
PROGESTERONEActive
Quantity: 100 mg in 1 1
Code: 4G7DS2Q64Y
Classification: ACTIB
GELATIN TYPE B BOVINE (160 BLOOM)Inactive
Code: 1T8387508X
Classification: IACT
LECITHIN, SOYBEANInactive
Code: 1DI56QDM62
Classification: IACT
FERROSOFERRIC OXIDEInactive
Code: XM0M87F357
Classification: IACT
PEANUT OILInactive
Code: 5TL50QU0W4
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
HYPROMELLOSE 2910 (6 MPA.S)Inactive
Code: 0WZ8WG20P6
Classification: IACT