Progesterone

Product NDC
76420-574
11-digit product format
764200574
Labeler code
76420
Product ID
76420-574_ffca6765-4ed7-292d-e053-6394a90a39f2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Progesterone
Dosage form
CAPSULE
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA205229
Marketing category
ANDA
Marketing start
2021-04-12
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
76420-574-0176420057401100 CAPSULE in 1 BOTTLE (76420-574-01) 100 capsule2023-07-06NoNoHistorical
76420-574-107642005741010 CAPSULE in 1 BOTTLE (76420-574-10) 10 capsule2023-07-06NoNoHistorical
76420-574-307642005743030 CAPSULE in 1 BOTTLE (76420-574-30) 30 capsule2023-07-06NoNoHistorical
76420-574-607642005746060 CAPSULE in 1 BOTTLE (76420-574-60) 60 capsule2023-07-06NoNoHistorical
76420-574-907642005749090 CAPSULE in 1 BOTTLE (76420-574-90) 90 capsule2023-07-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Progesterone CapsulesAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2023-07-06HUMAN PRESCRIPTION DRUG LABEL2