Medroxyprogesterone Acetate

Product NDC
50090-4251
11-digit product format
500904251
Labeler code
50090
Product ID
50090-4251_a4b97dc5-1bba-421d-b9e2-d71ef1c80302
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Medroxyprogesterone acetate
Dosage form
INJECTION, SUSPENSION, EXTENDED RELEASE
Route
INTRAMUSCULAR
Labeler
A-S Medication Solutions
Application
ANDA077235
Marketing category
ANDA
Marketing start
2017-11-28
Marketing end
0000-00-00
Substance
MEDROXYPROGESTERONE ACETATE
Active strength
150 mg/mL
Pharmacologic classes
Progesterone Congeners [CS],Progestin [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-4251-02023-02-07C16284748780-1f386c64a-3540-0266-e053-dadaa90a7c1aa67023c9-9927-4333-aa88-00804db36570
50090-4251-02023-01-30C16284748780-1f386c64a-3540-0266-e053-dadaa90a7c1aa67023c9-9927-4333-aa88-00804db36570

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-4251-0ML - Milliliter50090-425178fadbb1-35e9-4399-9963-59f4bc75465f12022-04-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-4251-0500904251001 VIAL, SINGLE-DOSE in 1 CARTON (50090-4251-0) > 1 mL in 1 VIAL, SINGLE-DOSE2019-04-030000-00-00NoNoCurrent