Alprazolam

Product NDC
49999-039
11-digit product format
499990039
Labeler code
49999
Product ID
49999-039_189cc961-c8a8-4706-8768-e1db58056c92
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ALPRAZOLAM
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA074112
Marketing category
ANDA
Marketing start
2010-04-01
Marketing end
0000-00-00
Substance
ALPRAZOLAM
Active strength
0 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
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
49999-039-10EA - Each49999-039474eab61-cf0f-41b9-80f5-3aace99a9b7e12012-07-24
49999-039-15EA - Each49999-03904b8269d-fa71-4de5-8d67-e4d2fd6e847212012-07-24
49999-039-30EA - Each49999-039fbfac82c-dd1f-4926-aab2-0dd5977b77bd12012-07-24
49999-039-60EA - Each49999-0395b87a83e-120a-495a-97bd-e02b498bb8cd12012-07-24
49999-039-90EA - Each49999-039403df5d5-6c7a-48de-9533-5a2f0e36f5c612012-07-24