AcipHex

Product NDC
23594-205
11-digit product format
235940205
Labeler code
23594
Product ID
23594-205_d57b1c4f-3a8e-ad37-e053-2a95a90ab9dc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
rabeprazole sodium
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Aytu Therapeutics, LLC
Application
NDA204736
Marketing category
NDA
Marketing start
2018-03-01
Marketing end
2022-01-31
Substance
RABEPRAZOLE SODIUM
Active strength
5 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
23594-205-01EA - Each23594-20543dc827a-4c82-448f-a867-48371e25febb12018-04-19

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
23594-205-012359402050130 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (23594-205-01) 2018-03-010000-00-00NoNoCurrent