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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

NDC Product Code71335-1443
Application NumberANDA211285
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateMay 20, 2021
Generic NameProgesterone

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
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Progesterone - FDA Approval | MedPath