Progesterone
Progesterone Capsules
Approved
Approval ID
96c59a1c-d562-46dd-868b-b2decdfef319
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 28, 2023
Manufacturers
FDA
A-S Medication Solutions
DUNS: 830016429
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 Code50090-6835
Application NumberANDA205229
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateApril 12, 2021
Generic NameProgesterone
INGREDIENTS (7)
PROGESTERONEActive
Quantity: 100 mg in 1 1
Code: 4G7DS2Q64Y
Classification: ACTIB
PEANUT OILInactive
Code: 5TL50QU0W4
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
GELATIN, UNSPECIFIEDInactive
Code: 2G86QN327L
Classification: IACT
LECITHIN, SOYBEANInactive
Code: 1DI56QDM62
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
MEDIUM-CHAIN TRIGLYCERIDESInactive
Code: C9H2L21V7U
Classification: IACT