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PHENDIMETRAZINE TARTRATE

NDC 68071-3509 · NuCare Pharmaceuticals,Inc.

Generic namePhendimetrazine Tartrate
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENDIMETRAZINE TARTRATE
Strength35 mg/1
Pharmacologic classAppetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
DEA scheduleCIII
Marketing categoryANDA

Packages

68071-3509-1 — 120 TABLET in 1 BOTTLE (68071-3509-1)

68071-3509-6 — 60 TABLET in 1 BOTTLE (68071-3509-6)

68071-3509-8 — 180 TABLET in 1 BOTTLE (68071-3509-8)

68071-3509-9 — 90 TABLET in 1 BOTTLE (68071-3509-9)

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, 68071-3839 — 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, 72989-409 — PHENDIMETRAZINE TARTRATE

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