Zolpidem Tartrate

Product NDC
63187-116
11-digit product format
631870116
Labeler code
63187
Product ID
63187-116_a8286d35-0074-4bfe-a82f-585c1b34ca3b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
zolpidem tartrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA078616
Marketing category
ANDA
Marketing start
2008-11-21
Marketing end
0000-00-00
Substance
ZOLPIDEM TARTRATE
Active strength
10 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
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
63187-116-30EA - Each63187-116bac7fa7f-3c4d-4e6a-b6d6-187e4544fca712015-06-09