Progesterone

Product NDC
71205-903
11-digit product format
712050903
Labeler code
71205
Product ID
71205-903_eb911dcf-c635-4133-9d70-db58b6636a97
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Progesterone
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA205229
Marketing category
ANDA
Marketing start
2021-01-08
Substance
PROGESTERONE
Active strength
200 mg/1
Pharmacologic classes
Progesterone [CS], Progesterone [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
4G7DS2Q64YPROGESTERONE57-83-0PROGESTERONE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71205-903-11712050903111000 CAPSULE in 1 BOTTLE (71205-903-11) 1000 capsule2021-07-20NoNoHistorical
71205-903-307120509033030 CAPSULE in 1 BOTTLE (71205-903-30) 30 capsule2021-07-20NoNoHistorical
71205-903-5571205090355500 CAPSULE in 1 BOTTLE (71205-903-55) 500 capsule2021-07-20NoNoHistorical
71205-903-607120509036060 CAPSULE in 1 BOTTLE (71205-903-60) 60 capsule2021-07-20NoNoHistorical
71205-903-7271205090372120 CAPSULE in 1 BOTTLE (71205-903-72) 120 capsule2021-07-20NoNoHistorical
71205-903-907120509039090 CAPSULE in 1 BOTTLE (71205-903-90) 90 capsule2021-07-20NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Progesterone CapsulesProficient Rx LP2022-04-01HUMAN PRESCRIPTION DRUG LABEL2