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Last Updated: March 26, 2026

Details for New Drug Application (NDA): 212141

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NDA 212141 describes SUCRALFATE, which is a drug marketed by Abon Pharms Llc, Amneal, Cosette, Glenmark Pharms Ltd, Hikma, Mylan, Padagis Us, Pd Partners, Strides Pharma, Vistapharm Llc, Amneal Pharms, Chartwell Rx, Teva, and Zydus Lifesciences, and is included in fourteen NDAs. It is available from forty-five suppliers. Additional details are available on the SUCRALFATE profile page.

The generic ingredient in SUCRALFATE is sucralfate. There are fourteen drug master file entries for this compound. Forty-eight suppliers are listed for this compound. Additional details are available on the sucralfate profile page.

Summary for 212141

Tradename:	SUCRALFATE
Applicant:	Glenmark Pharms Ltd
Ingredient:	sucralfate
Patents:	0

Pharmacology for NDA: 212141

Medical Subject Heading (MeSH) Categories for 212141

Anti-Ulcer Agents

Suppliers and Packaging for NDA: 212141

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
SUCRALFATE	sucralfate	SUSPENSION;ORAL	212141	ANDA	Glenmark Pharmaceuticals Inc., USA	68462-827	68462-827-61	420 mL in 1 BOTTLE (68462-827-61)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SUSPENSION;ORAL			Strength	1GM/10ML
Approval Date:	Jan 5, 2026	TE:	AB	RLD:	No

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