Progesterone
Progesterone Capsules
Approved
Approval ID
80a63b2b-96be-423d-abbd-13acc802f6da
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 1, 2022
Manufacturers
FDA
Proficient Rx LP
DUNS: 079196022
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 Code71205-669
Application NumberANDA205229
Product Classification
M
Marketing Category
C73584
G
Generic Name
Progesterone
Product Specifications
Route of AdministrationORAL
Effective DateJune 1, 2022
FDA Product Classification
INGREDIENTS (7)
PROGESTERONEActive
Quantity: 200 mg in 1 1
Code: 4G7DS2Q64Y
Classification: ACTIB
PEANUT OILInactive
Code: 5TL50QU0W4
Classification: IACT
GELATIN, UNSPECIFIEDInactive
Code: 2G86QN327L
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
LECITHIN, SOYBEANInactive
Code: 1DI56QDM62
Classification: IACT
MEDIUM-CHAIN TRIGLYCERIDESInactive
Code: C9H2L21V7U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT