Last Updated: November 8, 2026

Details for New Drug Application (NDA): 214735

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NDA 214735 describes GLYCOPYRROLATE, which is a drug marketed by Abraxis Pharm, Accord Hlthcare, Alembic, Am Regent, Amneal, Apotex, Caplin, Eugia Pharma, Fresenius Kabi Usa, Gland, Hikma Farmaceutica, Hospira, Lupin, Mankind Pharma, Meitheal, Nivagen, Omnivium Pharms, Piramal Critical, Prinston Inc, Sagent, Sandoz, Somerset Theraps Llc, Teva Parenteral, Watson Labs, Xiromed, Zydus Pharms, Ajenat Pharms, Annora Pharma, Aurobindo Pharma Ltd, Bionpharma, Chartwell Rx, Cohance Lifesciences, Granules, MSN, Ph Health, Quagen, Sciegen Pharms, Appco, Aurobindo Pharma, Hikma, Lgm Pharma, Natco, Regcon Holdings, Rising, Sun Pharm Inds Ltd, Tp Anda Holdings, and Velzen Pharma Pvt, and is included in sixty NDAs. It is available from fifty-eight suppliers. Additional details are available on the GLYCOPYRROLATE profile page.

The generic ingredient in GLYCOPYRROLATE is glycopyrrolate. There is one drug master file entry for this compound. Sixty-one suppliers are listed for this compound. Additional details are available on the glycopyrrolate profile page.

Summary for 214735

Tradename:	GLYCOPYRROLATE
Applicant:	Granules
Ingredient:	glycopyrrolate
Patents:	0

Pharmacology for NDA: 214735

Mechanism of Action	Cholinergic Antagonists Cholinergic Muscarinic Antagonists

Medical Subject Heading (MeSH) Categories for 214735

Adjuvants, Anesthesia
Muscarinic Antagonists

Suppliers and Packaging for NDA: 214735

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
GLYCOPYRROLATE	glycopyrrolate	SOLUTION;ORAL	214735	ANDA	Granules Pharmaceuticals Inc.	70010-106	70010-106-44	473 mL in 1 BOTTLE (70010-106-44)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;ORAL			Strength	1MG/5ML
Approval Date:	Aug 19, 2024	TE:	AA	RLD:	No

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