PROGESTERONE

Product NDC
82804-268
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PROGESTERONE
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA200900
Marketing category
ANDA
Substance
PROGESTERONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
82804-268-3030 CAPSULE in 1 BOTTLE (82804-268-30) 2026-02-19NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Bionpharma-Progesterone capsulesProficient Rx LP2026-02-01HUMAN PRESCRIPTION DRUG LABEL1