Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate

Product NDC
71335-0699
11-digit product format
713350699
Labeler code
71335
Product ID
71335-0699_a860e145-17c2-4045-9edf-4e8d9641ad01
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040439
Marketing category
ANDA
Marketing start
2002-06-14
Marketing end
0000-00-00
Substance
AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Active strength
5 mg/1; mg/1; mg/1; mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC], Central Nervous System Stimulant [EPC], Central Nervous System Stimulant [EPC], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Central Nervous System Stimulation [PE], Central Nervous System Stimulation [PE], Central Nervous System Stimulation [PE]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0699-17133506990160 TABLET in 1 BOTTLE (71335-0699-1) 60 tablet2018-02-220000-00-00NoNoCurrent
71335-0699-27133506990290 TABLET in 1 BOTTLE (71335-0699-2) 90 tablet2019-05-150000-00-00NoNoCurrent
71335-0699-37133506990330 TABLET in 1 BOTTLE (71335-0699-3) 30 tablet2018-02-200000-00-00NoNoCurrent
71335-0699-471335069904120 TABLET in 1 BOTTLE (71335-0699-4) 120 tablet2022-02-140000-00-00NoNoCurrent
71335-0699-57133506990518 TABLET in 1 BOTTLE (71335-0699-5) 18 tablet2022-02-140000-00-00NoNoCurrent