NDC 71335-0646 – Phentermine hydrochloride

Phentermine Hydrochloride 37.5 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-0646

Product details

Brand name
Phentermine hydrochloride
Generic name
Phentermine hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA205017
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
71335-0646-056 CAPSULE in 1 BOTTLE (71335-0646-0)Dec 17, 2018
71335-0646-114 CAPSULE in 1 BOTTLE (71335-0646-1)Feb 12, 2018
71335-0646-27 CAPSULE in 1 BOTTLE (71335-0646-2)Jul 6, 2018
71335-0646-330 CAPSULE in 1 BOTTLE (71335-0646-3)Feb 12, 2018
71335-0646-450 CAPSULE in 1 BOTTLE (71335-0646-4)Jan 28, 2025
71335-0646-590 CAPSULE in 1 BOTTLE (71335-0646-5)Jan 28, 2025
71335-0646-6120 CAPSULE in 1 BOTTLE (71335-0646-6)Jan 28, 2025
71335-0646-721 CAPSULE in 1 BOTTLE (71335-0646-7)Jan 28, 2025
71335-0646-828 CAPSULE in 1 BOTTLE (71335-0646-8)Feb 24, 2020
71335-0646-960 CAPSULE in 1 BOTTLE (71335-0646-9)Jan 28, 2025

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