Sumatriptan And Naproxen Sodium 47335-0410-22

Package NDC

47335-0410-22

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 20, 2018
Listing Expires: December 31, 2026
Application: ANDA202803

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Active Ingredients

Ingredient	Strength
Naproxen Sodium	500 mg/1
Sumatriptan Succinate	85 mg/1

Drug Class

Anti-Inflammatory AgentsNon-Steroidal [CS]Cyclooxygenase Inhibitors [MoA]

Selected Package

47335-0410-22Selected

9 TABLET, FILM COATED in 1 BOTTLE (47335-410-22)

Other packages for this product(2)

47335-0410-83

30 TABLET, FILM COATED in 1 BOTTLE (47335-410-83)

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47335-0410-88

100 TABLET, FILM COATED in 1 BOTTLE (47335-410-88)

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