NDC 63629-4385 – Phentermine Hydrochloride

Phentermine Hydrochloride 37.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC63629-4385

Product details

Brand name
Phentermine Hydrochloride
Generic name
Phentermine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040876
Marketed since
August 15, 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 (9)

Package NDCDescriptionSince
63629-4385-17 TABLET in 1 BOTTLE (63629-4385-1)Apr 2, 2024
63629-4385-230 TABLET in 1 BOTTLE (63629-4385-2)Apr 2, 2024
63629-4385-314 TABLET in 1 BOTTLE (63629-4385-3)Dec 24, 2012
63629-4385-460 TABLET in 1 BOTTLE (63629-4385-4)Apr 2, 2024
63629-4385-528 TABLET in 1 BOTTLE (63629-4385-5)Apr 18, 2013
63629-4385-624 TABLET in 1 BOTTLE (63629-4385-6)Mar 22, 2013
63629-4385-745 TABLET in 1 BOTTLE (63629-4385-7)May 10, 2016
63629-4385-890 TABLET in 1 BOTTLE (63629-4385-8)Dec 4, 2020
63629-4385-921 TABLET in 1 BOTTLE (63629-4385-9)Dec 18, 2015

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