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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 216726

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NDA 216726 describes SUCRALFATE, which is a drug marketed by Abon Pharms Llc, Amneal, Hikma, Mylan, Pd Partners, Strides Pharma, Vistapharm Llc, Amneal Pharms, Nostrum Labs Inc, Teva, and Zydus Lifesciences, and is included in eleven NDAs. It is available from thirty-seven 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-three suppliers are listed for this compound. Additional details are available on the sucralfate profile page.

Summary for 216726

Tradename:	SUCRALFATE
Applicant:	Abon Pharms Llc
Ingredient:	sucralfate
Patents:	0

Pharmacology for NDA: 216726

Medical Subject Heading (MeSH) Categories for 216726

Anti-Ulcer Agents

Suppliers and Packaging for NDA: 216726

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
SUCRALFATE	sucralfate	SUSPENSION;ORAL	216726	ANDA	Ingenus Pharmaceuticals, LLC	50742-386	50742-386-42	420 mL in 1 BOTTLE (50742-386-42)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SUSPENSION;ORAL			Strength	1GM/10ML
Approval Date:	Mar 21, 2024	TE:	AB	RLD:	No

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