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GLYCOPYRROLATE

NDC 70752-109 · QUAGEN PHARMACEUTICALS LLC

Generic nameGLYCOPYRROLATE
Dosage formTABLET
RouteORAL
Active ingredient(s)GLYCOPYRROLATE
Strength2 mg/1
Pharmacologic classAnticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
Marketing categoryANDA

Packages

70752-109-10 — 100 TABLET in 1 BOTTLE, PLASTIC (70752-109-10)

70752-109-11 — 1000 TABLET in 1 BOTTLE, PLASTIC (70752-109-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4597 — Glycopyrrolate, 70518-4671 — GLYCOPYRROLATE, 70700-165 — Glycopyrrolate, 70700-166 — Glycopyrrolate, 70700-167 — Glycopyrrolate, 70700-168 — Glycopyrrolate, 70700-264 — Glycopyrrolate, 70700-902 — Glycopyrrolate, 70700-903 — Glycopyrrolate, 70752-108 — GLYCOPYRROLATE, 70756-631 — Glycopyrrolate, 70756-632 — Glycopyrrolate, 70756-633 — Glycopyrrolate, 70756-634 — Glycopyrrolate, 71288-414 — Glycopyrrolate, 71288-415 — Glycopyrrolate, 71335-1225 — GLYCOPYRROLATE, 71335-2075 — Glycopyrrolate, 71335-2119 — glycopyrrolate, 71335-2720 — 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.