Progesterone

Product NDC
71335-1430
11-digit product format
713351430
Labeler code
71335
Product ID
71335-1430_b408d92e-73f7-4d71-9f4f-334906406a62
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Progesterone
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA207724
Marketing category
ANDA
Marketing start
2017-09-11
Marketing end
0000-00-00
Substance
PROGESTERONE
Active strength
100 mg/1
Pharmacologic classes
Progesterone [CS], Progesterone [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1430-17133514300130 CAPSULE in 1 BOTTLE (71335-1430-1) 30 capsule2019-12-110000-00-00NoNoCurrent
71335-1430-2713351430028 CAPSULE in 1 BOTTLE (71335-1430-2) 8 capsule2019-12-110000-00-00NoNoCurrent
71335-1430-371335143003100 CAPSULE in 1 BOTTLE (71335-1430-3) 100 capsule2019-12-110000-00-00NoNoCurrent
71335-1430-47133514300410 CAPSULE in 1 BOTTLE (71335-1430-4) 10 capsule2019-12-110000-00-00NoNoCurrent
71335-1430-57133514300590 CAPSULE in 1 BOTTLE (71335-1430-5) 90 capsule2019-12-110000-00-00NoNoCurrent
71335-1430-67133514300660 CAPSULE in 1 BOTTLE (71335-1430-6) 60 capsule2019-12-110000-00-00NoNoCurrent
71335-1430-77133514300712 CAPSULE in 1 BOTTLE (71335-1430-7) 12 capsule2021-12-280000-00-00NoNoCurrent