Manufacturing Establishments1
FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.
Proficient Rx LP
Proficient Rx LP
079196022
Products1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Progesterone
Product Details
NDC Product Code
71205-669Application Number
ANDA205229Marketing Category
ANDA (C73584)Route of Administration
ORALEffective Date
June 1, 2022ProgesteroneActive
Code: 4G7DS2Q64YClass: ACTIBQuantity: 200 mg in 1 1
PEANUT OILInactive
Code: 5TL50QU0W4Class: IACT
GELATIN, UNSPECIFIEDInactive
Code: 2G86QN327LClass: IACT
GLYCERINInactive
Code: PDC6A3C0OXClass: IACT
LECITHIN, SOYBEANInactive
Code: 1DI56QDM62Class: IACT
MEDIUM-CHAIN TRIGLYCERIDESInactive
Code: C9H2L21V7UClass: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JPClass: IACT