Phendimetrazine Tartrate

Product NDC
71335-2135
11-digit product format
713352135
Labeler code
71335
Product ID
71335-2135_69bf456e-4735-4d22-86bd-ff032525cc9d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phendimetrazine Tartrate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091042
Marketing category
ANDA
Marketing start
2010-09-15
Marketing end
0000-00-00
Substance
PHENDIMETRAZINE TARTRATE
Active strength
35 mg/1
Pharmacologic classes
Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
DEA schedule
CIII
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-2135-071335213500120 TABLET in 1 BOTTLE (71335-2135-0) 120 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-17133521350130 TABLET in 1 BOTTLE (71335-2135-1) 30 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-27133521350290 TABLET in 1 BOTTLE (71335-2135-2) 90 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-37133521350315 TABLET in 1 BOTTLE (71335-2135-3) 15 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-47133521350460 TABLET in 1 BOTTLE (71335-2135-4) 60 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-5713352135057 TABLET in 1 BOTTLE (71335-2135-5) 7 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-67133521350621 TABLET in 1 BOTTLE (71335-2135-6) 21 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-77133521350742 TABLET in 1 BOTTLE (71335-2135-7) 42 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-871335213508100 TABLET in 1 BOTTLE (71335-2135-8) 100 tablet2022-08-020000-00-00NoNoCurrent
71335-2135-97133521350928 TABLET in 1 BOTTLE (71335-2135-9) 28 tablet2022-08-020000-00-00NoNoCurrent