Alosetron Hydrochloride

Product NDC
42291-123
11-digit product format
422910123
Labeler code
42291
Product ID
42291-123_91c0dde8-6242-1f38-e053-2995a90adfea
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Alosetron Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
AvKARE, Inc.
Application
ANDA206647
Marketing category
ANDA
Marketing start
2017-02-23
Marketing end
0000-00-00
Substance
ALOSETRON HYDROCHLORIDE
Active strength
1 mg/1
Pharmacologic classes
Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42291-123-30EA - Each42291-1236d48bae9-4cff-499a-9750-feacdec047c012017-04-05