Progesterone

Product NDC
71205-902
11-digit product format
712050902
Labeler code
71205
Product ID
71205-902_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
100 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
71205-902-11712050902111000 CAPSULE in 1 BOTTLE (71205-902-11) 1000 capsule2021-07-20NoNoHistorical
71205-902-307120509023030 CAPSULE in 1 BOTTLE (71205-902-30) 30 capsule2021-07-20NoNoHistorical
71205-902-5571205090255500 CAPSULE in 1 BOTTLE (71205-902-55) 500 capsule2021-07-20NoNoHistorical
71205-902-607120509026060 CAPSULE in 1 BOTTLE (71205-902-60) 60 capsule2021-07-20NoNoHistorical
71205-902-7271205090272120 CAPSULE in 1 BOTTLE (71205-902-72) 120 capsule2021-07-20NoNoHistorical
71205-902-907120509029090 CAPSULE in 1 BOTTLE (71205-902-90) 90 capsule2021-07-20NoNoHistorical

Related DailyMed Labels

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