NDC 71335-3107 – Phentermine hydrochloride

Phentermine Hydrochloride 37.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-3107

Product details

Brand name
Phentermine hydrochloride
Generic name
Phentermine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205008
Marketed since
January 24, 2017
Listing expires
December 31, 2027
Pharmacologic class
Sympathomimetic Amine Anorectic

Active ingredients

Uses, dosage, side effects and warnings for Phentermine Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
71335-3107-090 TABLET in 1 BOTTLE (71335-3107-0)Mar 16, 2026
71335-3107-130 TABLET in 1 BOTTLE (71335-3107-1)Mar 16, 2026
71335-3107-215 TABLET in 1 BOTTLE (71335-3107-2)Mar 16, 2026
71335-3107-328 TABLET in 1 BOTTLE (71335-3107-3)Mar 16, 2026
71335-3107-47 TABLET in 1 BOTTLE (71335-3107-4)Mar 16, 2026
71335-3107-514 TABLET in 1 BOTTLE (71335-3107-5)Mar 16, 2026
71335-3107-660 TABLET in 1 BOTTLE (71335-3107-6)Mar 16, 2026
71335-3107-745 TABLET in 1 BOTTLE (71335-3107-7)Mar 16, 2026
71335-3107-82 TABLET in 1 BOTTLE (71335-3107-8)Mar 16, 2026
71335-3107-921 TABLET in 1 BOTTLE (71335-3107-9)Mar 16, 2026

Other Phentermine Hydrochloride products