NDC 71335-1860 – Phentermine Hydrochloride

Phentermine Hydrochloride 15 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1860

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, 2026
Pharmacologic class
Sympathomimetic Amine Anorectic

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1860-045 CAPSULE in 1 BOTTLE (71335-1860-0)Oct 21, 2021
71335-1860-17 CAPSULE in 1 BOTTLE (71335-1860-1)Oct 21, 2021
71335-1860-214 CAPSULE in 1 BOTTLE (71335-1860-2)Oct 21, 2021
71335-1860-330 CAPSULE in 1 BOTTLE (71335-1860-3)Oct 21, 2021
71335-1860-4100 CAPSULE in 1 BOTTLE (71335-1860-4)Oct 21, 2021
71335-1860-52 CAPSULE in 1 BOTTLE (71335-1860-5)Oct 21, 2021
71335-1860-628 CAPSULE in 1 BOTTLE (71335-1860-6)Oct 21, 2021
71335-1860-790 CAPSULE in 1 BOTTLE (71335-1860-7)Oct 21, 2021
71335-1860-821 CAPSULE in 1 BOTTLE (71335-1860-8)Oct 21, 2021
71335-1860-960 CAPSULE in 1 BOTTLE (71335-1860-9)Oct 21, 2021

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