Zaleplon

Product NDC
71335-1466
11-digit product format
713351466
Labeler code
71335
Product ID
71335-1466_5482ea84-3aa9-4d4d-9344-f51a6998dca4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Zaleplon
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090374
Marketing category
ANDA
Marketing start
2018-06-20
Marketing end
0000-00-00
Substance
ZALEPLON
Active strength
5 mg/1
Pharmacologic classes
Central Nervous System Depression [PE], GABA A Agonists [MoA], gamma-Aminobutyric Acid A Receptor Agonist [EPC]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1466-17133514660130 CAPSULE in 1 BOTTLE (71335-1466-1) 30 capsule2018-06-200000-00-00NoNoCurrent
71335-1466-27133514660260 CAPSULE in 1 BOTTLE (71335-1466-2) 60 capsule2018-06-200000-00-00NoNoCurrent
71335-1466-37133514660390 CAPSULE in 1 BOTTLE (71335-1466-3) 90 capsule2018-06-200000-00-00NoNoCurrent
71335-1466-47133514660420 CAPSULE in 1 BOTTLE (71335-1466-4) 20 capsule2018-06-200000-00-00NoNoCurrent
71335-1466-57133514660528 CAPSULE in 1 BOTTLE (71335-1466-5) 28 capsule2018-06-200000-00-00NoNoCurrent