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Glycopyrrolate

NDC 23155-606 · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Generic nameGlycopyrrolate
Dosage formTABLET
RouteORAL
Active ingredient(s)GLYCOPYRROLATE
Strength1 mg/1
Pharmacologic classAnticholinergic [EPC], Cholinergic Antagonists [MoA]
Marketing categoryANDA

Packages

23155-606-01 — 100 TABLET in 1 BOTTLE (23155-606-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13107-015 — GLYCOPYRROLATE, 15955-305 — GLYCOPYRROLATE, 15955-318 — GLYCOPYRROLATE, 16571-743 — Glycopyrrolate, 16571-744 — Glycopyrrolate, 16729-471 — glycopyrrolate, 16729-472 — glycopyrrolate, 16729-473 — glycopyrrolate, 16729-474 — glycopyrrolate, 17856-1016 — Glycopyrrolate, 23155-607 — Glycopyrrolate, 25021-796 — Glycopyrrolate, 31722-016 — Glycopyrrolate, 42023-269 — neostigmine methylsulfate and glycopyrrolate, 43547-543 — glycopyrrolate, 43547-544 — glycopyrrolate, 43547-639 — glycopyrrolate, 43547-640 — glycopyrrolate, 49884-042 — Glycopyrrolate, 49884-065 — glycopyrrolate, +177 more

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