NDC 71335-0161 – Phentermine Hydrochloride

Phentermine Hydrochloride 37.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-0161

Product details

Brand name
Phentermine Hydrochloride
Generic name
Phentermine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA200272
Marketed since
March 8, 2011
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
71335-0161-090 TABLET in 1 BOTTLE (71335-0161-0)Mar 8, 2011
71335-0161-130 TABLET in 1 BOTTLE (71335-0161-1)Mar 8, 2011
71335-0161-215 TABLET in 1 BOTTLE (71335-0161-2)Mar 8, 2011
71335-0161-328 TABLET in 1 BOTTLE (71335-0161-3)Mar 8, 2011
71335-0161-47 TABLET in 1 BOTTLE (71335-0161-4)Mar 8, 2011
71335-0161-514 TABLET in 1 BOTTLE (71335-0161-5)Mar 8, 2011
71335-0161-660 TABLET in 1 BOTTLE (71335-0161-6)Mar 8, 2011
71335-0161-745 TABLET in 1 BOTTLE (71335-0161-7)Mar 8, 2011
71335-0161-82 TABLET in 1 BOTTLE (71335-0161-8)Mar 8, 2011
71335-0161-921 TABLET in 1 BOTTLE (71335-0161-9)Mar 8, 2011

Other Phentermine Hydrochloride products