Alprazolam

Product NDC
55700-312
11-digit product format
557000312
Labeler code
55700
Product ID
55700-312_3a818102-611e-4ff9-ac54-a0b11dd774fb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Alprazolam
Dosage form
TABLET
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA074174
Marketing category
ANDA
Marketing start
2015-10-09
Marketing end
0000-00-00
Substance
ALPRAZOLAM
Active strength
1 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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-312-30EA - Each55700-312d0f6b2aa-cfbb-464c-befc-91f7edd09dff12018-12-13
55700-312-60EA - Each55700-31207935d84-8e4d-4947-a521-d66a4a5585df12018-12-13
55700-312-90EA - Each55700-312ceff06e3-e31c-429f-9bb8-5b937de4015c12018-12-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-312-305570003123030 TABLET in 1 BOTTLE (55700-312-30) 30 tablet2015-10-090000-00-00NoNoCurrent
55700-312-605570003126060 TABLET in 1 BOTTLE (55700-312-60) 60 tablet2015-10-090000-00-00NoNoCurrent
55700-312-905570003129090 TABLET in 1 BOTTLE (55700-312-90) 90 tablet2015-10-090000-00-00NoNoCurrent