NDC 71335-1840 – Phendimetrazine Tartrate

Phendimetrazine Tartrate 35 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIII

Product NDC71335-1840

Product details

Brand name
Phendimetrazine Tartrate
Generic name
Phendimetrazine Tartrate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA085588
Marketed since
July 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic Amine Anorectic

Active ingredients

Uses, dosage, side effects and warnings for Phendimetrazine Tartrate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1840-0120 TABLET in 1 BOTTLE (71335-1840-0)Jan 30, 2025
71335-1840-130 TABLET in 1 BOTTLE (71335-1840-1)Jan 30, 2025
71335-1840-290 TABLET in 1 BOTTLE (71335-1840-2)Jan 30, 2025
71335-1840-315 TABLET in 1 BOTTLE (71335-1840-3)Jan 30, 2025
71335-1840-460 TABLET in 1 BOTTLE (71335-1840-4)Jan 30, 2025
71335-1840-57 TABLET in 1 BOTTLE (71335-1840-5)Jan 30, 2025
71335-1840-621 TABLET in 1 BOTTLE (71335-1840-6)Jan 30, 2025
71335-1840-742 TABLET in 1 BOTTLE (71335-1840-7)Jan 30, 2025
71335-1840-8100 TABLET in 1 BOTTLE (71335-1840-8)Jan 30, 2025
71335-1840-928 TABLET in 1 BOTTLE (71335-1840-9)Jan 30, 2025

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