Glycopyrrolate

NDC 0781-3825 · Sandoz Inc

Generic nameGlycopyrrolate

Dosage formINJECTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)GLYCOPYRROLATE

Strength.2 mg/mL

Pharmacologic classAnticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

Marketing categoryANDA

Packages

0781-3825-96 — 25 VIAL in 1 CARTON (0781-3825-96) / 1 mL in 1 VIAL (0781-3825-71)

Billed under HCPCS

J1596 — Injection, glycopyrrolate, 0.1 mg Medicare Part B payment limit (ASP + 6%): $0.36

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0404-9777 — Glycopyrrolate, 0404-9782 — Glycopyrrolate, 0404-9867 — GLYCOPYRROLATE, 0517-4601 — Glycopyrrolate, 0517-4602 — Glycopyrrolate, 0517-4605 — Glycopyrrolate, 0517-4620 — Glycopyrrolate, 0615-8617 — GLYCOPYRROLATE, 0641-6212 — Glycopyrrolate, 0641-6213 — 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, 13107-015 — GLYCOPYRROLATE, +177 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.