Dutasteride

Product NDC
50090-3040
11-digit product format
500903040
Labeler code
50090
Product ID
50090-3040_3a124aff-f592-494f-ba4c-4293676cc389
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dutasteride
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA203118
Marketing category
ANDA
Marketing start
2015-11-02
Marketing end
0000-00-00
Substance
DUTASTERIDE
Active strength
1 mg/1
Pharmacologic classes
5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-3040-0EA - Each50090-3040162514d5-4725-45f5-980b-ab67bee52ea812019-05-02