NDC 71335-0678 – Phentermine Hydrochloride

Phentermine Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-0678

Product details

Brand name
Phentermine Hydrochloride
Generic name
Phentermine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA040886
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 (10)

Package NDCDescriptionSince
71335-0678-024 CAPSULE in 1 BOTTLE (71335-0678-0)May 30, 2024
71335-0678-130 CAPSULE in 1 BOTTLE (71335-0678-1)May 30, 2024
71335-0678-27 CAPSULE in 1 BOTTLE (71335-0678-2)May 30, 2024
71335-0678-314 CAPSULE in 1 BOTTLE (71335-0678-3)May 30, 2024
71335-0678-456 CAPSULE in 1 BOTTLE (71335-0678-4)May 30, 2024
71335-0678-560 CAPSULE in 1 BOTTLE (71335-0678-5)May 30, 2024
71335-0678-62 CAPSULE in 1 BOTTLE (71335-0678-6)May 30, 2024
71335-0678-721 CAPSULE in 1 BOTTLE (71335-0678-7)May 30, 2024
71335-0678-828 CAPSULE in 1 BOTTLE (71335-0678-8)May 30, 2024
71335-0678-942 CAPSULE in 1 BOTTLE (71335-0678-9)May 30, 2024

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