NDC 71335-3017 – Phentermine Hydrochloride

Phentermine Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-3017

Product details

Brand name
Phentermine Hydrochloride
Generic name
Phentermine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA205019
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 (6)

Package NDCDescriptionSince
71335-3017-130 CAPSULE in 1 BOTTLE (71335-3017-1)Feb 4, 2026
71335-3017-242 CAPSULE in 1 BOTTLE (71335-3017-2)Feb 4, 2026
71335-3017-314 CAPSULE in 1 BOTTLE (71335-3017-3)Feb 4, 2026
71335-3017-420 CAPSULE in 1 BOTTLE (71335-3017-4)Feb 4, 2026
71335-3017-528 CAPSULE in 1 BOTTLE (71335-3017-5)Feb 4, 2026
71335-3017-660 CAPSULE in 1 BOTTLE (71335-3017-6)Feb 4, 2026

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