NDC 71335-0350 – Phentermine Hydrochloride

Phentermine Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-0350

Product details

Brand name
Phentermine Hydrochloride
Generic name
Phentermine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040526
Marketed since
August 12, 2013
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
71335-0350-090 TABLET in 1 BOTTLE (71335-0350-0)Nov 20, 2018
71335-0350-17 TABLET in 1 BOTTLE (71335-0350-1)Apr 10, 2018
71335-0350-214 TABLET in 1 BOTTLE (71335-0350-2)Mar 12, 2018
71335-0350-315 TABLET in 1 BOTTLE (71335-0350-3)Mar 20, 2018
71335-0350-428 TABLET in 1 BOTTLE (71335-0350-4)Apr 2, 2018
71335-0350-530 TABLET in 1 BOTTLE (71335-0350-5)Mar 27, 2018
71335-0350-645 TABLET in 1 BOTTLE (71335-0350-6)Mar 13, 2018
71335-0350-760 TABLET in 1 BOTTLE (71335-0350-7)Apr 6, 2018
71335-0350-842 TABLET in 1 BOTTLE (71335-0350-8)Apr 9, 2018
71335-0350-956 TABLET in 1 BOTTLE (71335-0350-9)Mar 26, 2018

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