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Glycopyrrolate Oral Solution

NDC 51672-5316 · Sun Pharmaceutical Industries, Inc.

Generic nameGlycopyrrolate Oral Solution
Dosage formLIQUID
RouteORAL
Active ingredient(s)GLYCOPYRROLATE
Strength1 mg/5mL
Pharmacologic classAnticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
Marketing categoryANDA

Packages

51672-5316-9 — 1 BOTTLE in 1 CARTON (51672-5316-9) / 500 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49884-042 — Glycopyrrolate, 49884-065 — glycopyrrolate, 49884-066 — glycopyrrolate, 50268-363 — Glycopyrrolate, 51662-1425 — GLYCOPYRROLATE, 51662-1431 — GLYCOPYRROLATE, 51662-1484 — GLYCOPYRROLATE, 51662-1487 — GLYCOPYRROLATE, 51662-1554 — GLYCOPYRROLATE, 51662-1601 — GLYCOPYRROLATE, 51754-6000 — glycopyrrolate, 51754-6001 — glycopyrrolate, 51754-6013 — glycopyrrolate, 51754-6015 — glycopyrrolate, 55111-648 — Glycopyrrolate, 55111-649 — Glycopyrrolate, 55150-292 — Glycopyrrolate, 55150-293 — Glycopyrrolate, 55150-294 — Glycopyrrolate, 55150-295 — 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.