NDC 13107-061 – Phentermine Hydrochloride

Phentermine Hydrochloride 37.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC13107-061

Product details

Brand name
Phentermine Hydrochloride
Generic name
Phentermine Hydrochloride
Labeler
Aurolife Pharma LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203068
Marketed since
April 10, 2026
Listing expires
December 31, 2027
Pharmacologic class
Sympathomimetic Amine Anorectic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
13107-061-01100 TABLET in 1 BOTTLE (13107-061-01)Apr 10, 2026
13107-061-3030 TABLET in 1 BOTTLE (13107-061-30)Apr 10, 2026
13107-061-991000 TABLET in 1 BOTTLE (13107-061-99)Apr 10, 2026

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