Alprazolam

Product NDC
50090-5257
11-digit product format
500905257
Labeler code
50090
Product ID
50090-5257_e21e75f7-8564-41f0-be0c-9ad4d46bdd71
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Alprazolam
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA207507
Marketing category
ANDA
Marketing start
2018-07-09
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
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2ffbe5ef-58ff-88b9-e291-045e0f861f4fProduct name420180827
1f9e6d58-49d3-d9c1-e570-4bb0466a2c0bProduct name120140508
a1a11520-f3e2-68fa-8bd9-e80b271ef797Product name120140508
d153678e-a3c8-bad8-cfe0-385656dde0e7Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-5257ALPRAZOLAM TABLET [A-S MEDICATION SOLUTIONS]13Legacy NDC20231229_2c3526eb-642a-4602-bdab-fd9065b4e694.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-5257-05009052570030 TABLET in 1 BOTTLE (50090-5257-0) 30 tablet2020-10-150000-00-00NoNoCurrent
50090-5257-45009052570490 TABLET in 1 BOTTLE (50090-5257-4) 90 tablet2020-10-150000-00-00NoNoCurrent