Glycopyrrolate

NDC 70069-011 · Somerset Therapeutics, LLC

Generic nameGlycopyrrolate

Dosage formINJECTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)GLYCOPYRROLATE

Strength.2 mg/mL

Pharmacologic classAnticholinergic [EPC], Cholinergic Antagonists [MoA]

Marketing categoryANDA

Packages

70069-011-25 — 25 VIAL in 1 CARTON (70069-011-25) / 1 mL in 1 VIAL (70069-011-01)

FDA lists these products with the same active ingredient.

68083-377 — Glycopyrrolate, 68083-378 — Glycopyrrolate, 68083-379 — Glycopyrrolate, 68094-073 — Glycopyrrolate, 69076-475 — GLYCOPYRROLATE, 69076-476 — GLYCOPYRROLATE, 69315-139 — Glycopyrrolate, 69315-140 — Glycopyrrolate, 69452-406 — glycopyrrolate, 70010-106 — Glycopyrrolate, 70069-012 — Glycopyrrolate, 70069-013 — Glycopyrrolate, 70069-014 — Glycopyrrolate, 70069-616 — GLYCOPYRROLATE, 70069-617 — GLYCOPYRROLATE, 70069-618 — GLYCOPYRROLATE, 70069-619 — GLYCOPYRROLATE, 70121-1394 — Glycopyrrolate, 70121-1395 — Glycopyrrolate, 70121-1396 — 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.