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PHENDIMETRAZINE TARTRATE

NDC 72989-409 · Acertis Pharmaceuticals, LLC

Generic namePHENDIMETRAZINE TARTRATE
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)PHENDIMETRAZINE TARTRATE
Strength105 mg/1
Pharmacologic classAppetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
DEA scheduleCIII
Marketing categoryNDA

Packages

72989-409-30 — 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72989-409-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10702-045 — Phendimetrazine Tartrate, 10702-077 — Phendimetrazine Tartrate, 10702-078 — Phendimetrazine Tartrate, 17224-800 — PHENDIMETRAZINE TARTRATE, 43063-510 — Phendimetrazine Tartrate, 50090-0715 — Phendimetrazine Tartrate, 50090-2235 — Phendimetrazine Tartrate, 50090-6552 — Phendimetrazine Tartrate, 63629-2489 — PHENDIMETRAZINE TARTRATE, 64850-440 — Phendimetrazine Tartrate, 66267-394 — Phendimetrazine Tartrate, 68071-3509 — Phendimetrazine Tartrate, 68071-3839 — Phendimetrazine Tartrate, 68788-7236 — Phendimetrazine Tartrate, 69543-410 — PHENDIMETRAZINE TARTRATE, 71335-0074 — Phendimetrazine Tartrate, 71335-0324 — Phendimetrazine Tartrate, 71335-1840 — PHENDIMETRAZINE TARTRATE, 72162-2044 — Phendimetrazine Tartrate

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