Home NDC 71335-0699
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 NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71335-0699-1 71335069901 60 TABLET in 1 BOTTLE (71335-0699-1) 60 tablet 2018-02-22 0000-00-00 No No Current 71335-0699-2 71335069902 90 TABLET in 1 BOTTLE (71335-0699-2) 90 tablet 2019-05-15 0000-00-00 No No Current 71335-0699-3 71335069903 30 TABLET in 1 BOTTLE (71335-0699-3) 30 tablet 2018-02-20 0000-00-00 No No Current 71335-0699-4 71335069904 120 TABLET in 1 BOTTLE (71335-0699-4) 120 tablet 2022-02-14 0000-00-00 No No Current 71335-0699-5 71335069905 18 TABLET in 1 BOTTLE (71335-0699-5) 18 tablet 2022-02-14 0000-00-00 No No Current