Progesterone

Product NDC
50090-6835
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Progesterone
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA205229
Marketing category
ANDA
Substance
PROGESTERONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6835-010 CAPSULE in 1 BOTTLE (50090-6835-0) 2023-11-21NoHistorical
50090-6835-190 CAPSULE in 1 BOTTLE (50090-6835-1) 2023-11-21NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Progesterone CapsulesA-S Medication Solutions2023-11-28HUMAN PRESCRIPTION DRUG LABEL1