Zolpidem Tartrate Extended Release

Product NDC
60760-116
11-digit product format
607600116
Labeler code
60760
Product ID
60760-116_77e68d0b-c9f6-b796-e053-2991aa0a3918
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ZOLPIDEM TARTRATE
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
St Marys Medical Park Pharmacy
Application
ANDA078148
Marketing category
ANDA
Marketing start
2013-01-10
Marketing end
2019-06-30
Substance
ZOLPIDEM TARTRATE
Active strength
13 mg/1
Pharmacologic classes
gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [CS],Central Nervous System Depression [PE]
DEA schedule
CIV
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
60760-116-30EA - Each60760-116eff9a03d-f4be-4ebb-8b31-dcf16f3a263e12013-02-13