Progesterone Injection

Product NDC
40042-050
11-digit product format
400420050
Labeler code
40042
Product ID
40042-050_dc3647a7-842f-46ab-8b42-d19e66a251e9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Progesterone Injection
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR
Labeler
PharmaForce, Inc.
Application
ANDA090845
Marketing category
ANDA
Marketing start
2009-09-04
Marketing end
0000-00-00
Substance
PROGESTERONE
Active strength
50 mg/mL
Pharmacologic classes
Progesterone [CS],Progesterone [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40042-050-102019-10-21C16284748780-1956f9ecf-c4e0-621f-e053-dbdaa90a74add06b170c-10ea-4cc5-aa6b-151ac9b1d400