NDC 71335-0564 – Phentermine Hydrochloride

Phentermine Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-0564

Product details

Brand name
Phentermine Hydrochloride
Generic name
Phentermine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA040875
Marketed since
August 7, 2012
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic Amine Anorectic

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-0564-130 CAPSULE in 1 BOTTLE (71335-0564-1)Feb 23, 2018
71335-0564-27 CAPSULE in 1 BOTTLE (71335-0564-2)Mar 6, 2018
71335-0564-342 CAPSULE in 1 BOTTLE (71335-0564-3)May 29, 2024
71335-0564-428 CAPSULE in 1 BOTTLE (71335-0564-4)Feb 27, 2019
71335-0564-560 CAPSULE in 1 BOTTLE (71335-0564-5)Mar 28, 2019
71335-0564-614 CAPSULE in 1 BOTTLE (71335-0564-6)Feb 5, 2018
71335-0564-721 CAPSULE in 1 BOTTLE (71335-0564-7)May 29, 2024
71335-0564-890 CAPSULE in 1 BOTTLE (71335-0564-8)May 29, 2024

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