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PHENTERMINE HYDROCHLORIDE

NDC 13107-061 · Aurolife Pharma LLC

Generic namePHENTERMINE HYDROCHLORIDE
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENTERMINE HYDROCHLORIDE
Strength37.5 mg/1
Pharmacologic classAppetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
DEA scheduleCIV
Marketing categoryANDA

Packages

13107-061-01 — 100 TABLET in 1 BOTTLE (13107-061-01)

13107-061-30 — 30 TABLET in 1 BOTTLE (13107-061-30)

13107-061-99 — 1000 TABLET in 1 BOTTLE (13107-061-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10702-025 — Phentermine Hydrochloride, 10702-026 — Phentermine Hydrochloride, 10702-027 — Phentermine Hydrochloride, 10702-028 — Phentermine Hydrochloride, 10702-029 — Phentermine Hydrochloride, 10702-067 — Phentermine Hydrochloride, 11534-157 — phentermine hydrochloride, 11534-159 — phentermine hydrochloride, 11534-160 — phentermine hydrochloride, 11534-176 — phentermine hydrochloride, 13107-105 — Phentermine Hydrochloride, 13107-106 — Phentermine Hydrochloride, 17224-840 — PHENTERMINE HYDROCHLORIDE, 17224-851 — PHENTERMINE HYDROCHLORIDE, 17224-870 — PHENTERMINE HYDROCHLORIDE, 17224-877 — PHENTERMINE HYDROCHLORIDE, 17224-890 — PHENTERMINE HYDROCHLORIDE, 17224-901 — PHENTERMINE HYDROCHLORIDE, 17224-902 — PHENTERMINE HYDROCHLORIDE, 17224-904 — PHENTERMINE HYDROCHLORIDE, +118 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.