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Glycopyrrolate

NDC 71921-111 · Florida Pharmaceutical Products, 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

71921-111-01 — 100 TABLET in 1 BOTTLE (71921-111-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71872-7179 — Glycopyrrolate, 71872-7181 — Glycopyrrolate, 71872-7196 — Glycopyrrolate, 71872-7208 — glycopyrrolate, 71872-7224 — Glycopyrrolate, 71872-7238 — glycopyrrolate, 71872-7289 — Glycopyrrolate, 71872-7292 — Glycopyrrolate, 71872-7307 — Glycopyrrolate, 71921-110 — Glycopyrrolate, 72162-1477 — glycopyrrolate, 72162-1478 — glycopyrrolate, 72162-2597 — GLYCOPYRROLATE, 72162-2598 — GLYCOPYRROLATE, 72205-070 — GLYCOPYRROLATE, 72572-225 — Glycopyrrolate, 72572-226 — Glycopyrrolate, 72603-240 — Glycopyrrolate, 72887-160 — GLYCOPYRROLATE, 75834-193 — 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.