Zaleplon

Product NDC
50436-1006
11-digit product format
504361006
Labeler code
50436
Product ID
50436-1006_e85ee5db-46e6-4b44-a456-3fcb5b8bc0fd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Zaleplon
Dosage form
CAPSULE
Route
ORAL
Labeler
Unit Dose Services
Application
ANDA077239
Marketing category
ANDA
Marketing start
2008-06-06
Marketing end
0000-00-00
Substance
ZALEPLON
Active strength
10 mg/1
Pharmacologic classes
gamma-Aminobutyric Acid A Receptor Agonist [EPC],GABA A Agonists [MoA],Central Nervous System Depression [PE]
DEA schedule
CIV
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
50436-1006-1EA - Each50436-10063a825615-196e-482c-a96d-c3f42e80f6c212013-02-13