Alprazolam

Product NDC
50090-5262
11-digit product format
500905262
Labeler code
50090
Product ID
50090-5262_2bfecfa5-db3f-4d2b-a824-dc60dc23ae77
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
2 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
50090-5262ALPRAZOLAM TABLET [A-S MEDICATION SOLUTIONS]7Legacy NDC20250108_4a1cf38c-f0d7-4907-a866-b37052a72624.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-5262-05009052620060 TABLET in 1 BOTTLE (50090-5262-0) 60 tablet2020-10-150000-00-00NoNoCurrent
50090-5262-15009052620190 TABLET in 1 BOTTLE (50090-5262-1) 90 tablet2020-10-150000-00-00NoNoCurrent