Droxidopa

Product NDC
0054-0534
11-digit product format
000540534
Labeler code
0054
Product ID
0054-0534_32e24bbf-d284-4365-9aab-947496046910
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Droxidopa
Dosage form
CAPSULE
Route
ORAL
Labeler
Hikma Pharmaceuticals USA Inc.
Application
ANDA212835
Marketing category
ANDA
Marketing start
2021-02-18
Marketing end
0000-00-00
Substance
DROXIDOPA
Active strength
300 mg/1
Pharmacologic classes
Catecholamines [CS],Increased Blood Pressure [PE]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0054-0534-22EA - Each0054-0534160f968a-0e46-4901-846f-750102763be512021-03-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0054-0534-220005405342290 CAPSULE in 1 BOTTLE (0054-0534-22) 90 capsule2021-02-180000-00-00NoNoCurrent