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Tolterodine Tartrate

NDC 31722-806 · Camber Pharmaceuticals, Inc.

Generic nameTolterodine Tartrate
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)TOLTERODINE TARTRATE
Strength2 mg/1
Pharmacologic classCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
Marketing categoryANDA

Packages

31722-806-01 — 10 BLISTER PACK in 1 CARTON (31722-806-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-806-31)

31722-806-02 — 10 BLISTER PACK in 1 CARTON (31722-806-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-806-32)

31722-806-05 — 500 TABLET, FILM COATED in 1 BOTTLE (31722-806-05)

31722-806-60 — 60 TABLET, FILM COATED in 1 BOTTLE (31722-806-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16571-127 — Tolterodine Tartrate, 27241-191 — Tolterodine tartrate, 27241-192 — Tolterodine tartrate, 29300-239 — Tolterodine Tartrate, 29300-240 — Tolterodine Tartrate, 29300-306 — Tolterodine tartrate, 29300-307 — Tolterodine tartrate, 31722-607 — Tolterodine Tartrate, 31722-608 — Tolterodine Tartrate, 31722-805 — Tolterodine Tartrate, 33342-097 — Tolterodine tartrate, 33342-098 — Tolterodine tartrate, 43975-322 — Tolterodine Tartrate, 43975-323 — Tolterodine Tartrate, 50090-3475 — Tolterodine Tartrate, 51407-739 — Tolterodine Tartrate, 51407-740 — Tolterodine Tartrate, 58151-098 — tolterodine tartrate, 58151-099 — tolterodine tartrate, 59762-0170 — Tolterodine Tartrate, +14 more

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