Estradiol and Progesterone

Product NDC
69238-1690
11-digit product format
692381690
Labeler code
69238
Product ID
69238-1690_1b3d036c-81d6-4373-a4f8-a324c9465d18
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Estradiol and Progesterone
Dosage form
CAPSULE
Route
ORAL
Labeler
Amneal Pharmaceuticals NY LLC
Application
ANDA214293
Marketing category
ANDA
Marketing start
2022-05-20
Marketing end
0000-00-00
Substance
ESTRADIOL; PROGESTERONE
Active strength
1 mg/1; mg/1
Pharmacologic classes
Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone [CS], Progesterone [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69238-1690ESTRADIOL AND PROGESTERONE CAPSULE [AMNEAL PHARMACEUTICALS NY LLC]9Legacy NDC20240616_08ac4bbb-49c3-4b76-989c-3cbb913c66ce.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69238-1690-3692381690031 BLISTER PACK in 1 CARTON (69238-1690-3) > 30 CAPSULE in 1 BLISTER PACK1 blister pack2022-05-200000-00-00NoNoCurrent