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Tolterodine Tartrate

NDC 70436-161 · Slate Run Pharmaceuticals, LLC

Generic nameTolterodine Tartrate
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)TOLTERODINE TARTRATE
Strength4 mg/1
Pharmacologic classCholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
Marketing categoryANDA

Packages

70436-161-02 — 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-161-02)

70436-161-04 — 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-161-04)

70436-161-06 — 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-161-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

29300-306 — Tolterodine tartrate, 29300-307 — Tolterodine tartrate, 31722-607 — Tolterodine Tartrate, 31722-608 — Tolterodine Tartrate, 31722-805 — Tolterodine Tartrate, 31722-806 — 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, 60687-319 — Tolterodine, 60687-330 — Tolterodine, 70436-160 — Tolterodine Tartrate, 71205-319 — 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.