Progesterone

Product NDC
71335-0825
11-digit product format
713350825
Labeler code
71335
Product ID
71335-0825_0ec6a28f-bc58-4a82-8b23-22c359000593
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Progesterone
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA200456
Marketing category
ANDA
Marketing start
2012-10-04
Marketing end
0000-00-00
Substance
PROGESTERONE
Active strength
200 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
71335-0825-17133508250130 CAPSULE in 1 BOTTLE (71335-0825-1) 30 capsule2018-05-150000-00-00NoNoCurrent
71335-0825-27133508250228 CAPSULE in 1 BOTTLE (71335-0825-2) 28 capsule2022-02-140000-00-00NoNoCurrent
71335-0825-37133508250318 CAPSULE in 1 BOTTLE (71335-0825-3) 18 capsule2021-12-270000-00-00NoNoCurrent
71335-0825-47133508250490 CAPSULE in 1 BOTTLE (71335-0825-4) 90 capsule2019-01-100000-00-00NoNoCurrent
71335-0825-571335082505100 CAPSULE in 1 BOTTLE (71335-0825-5) 100 capsule2021-12-270000-00-00NoNoCurrent
71335-0825-6713350825066 CAPSULE in 1 BOTTLE (71335-0825-6) 6 capsule2022-02-140000-00-00NoNoCurrent
71335-0825-77133508250760 CAPSULE in 1 BOTTLE (71335-0825-7) 60 capsule2022-02-140000-00-00NoNoCurrent