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GLYCOPYRROLATE

NDC 13107-015 · Aurolife Pharma 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

13107-015-01 — 100 TABLET in 1 BOTTLE (13107-015-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0781-3825 — Glycopyrrolate, 0781-3827 — Glycopyrrolate, 0781-3829 — Glycopyrrolate, 0781-3831 — Glycopyrrolate, 0904-6709 — Glycopyrrolate, 10122-120 — beclomethasone dipropionate/formoterol fumarate/glycopyrrolate, 10122-121 — beclomethasone dipropionate/formoterol fumarate/glycopyrrolate, 10122-460 — beclomethasone dipropionate/formoterol fumarate/glycopyrrolate, 10122-590 — beclomethasone dipropionate/formoterol fumarate/glycopyrrolate, 13107-014 — 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, 23155-606 — 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.