Sodium Phenylbutyrate 68462-0853-20

Package NDC

68462-0853-20

Manufacturer: Glenmark Pharmaceuticals Inc., Usa
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 1, 2022
Listing Expires: December 31, 2027
Application: ANDA216462

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Active Ingredients

Ingredient	Strength
Sodium Phenylbutyrate	500 mg/1

Drug Class

Ammonium Ion Binding Activity [MoA]Nitrogen Binding Agent [EPC]

Selected Package

68462-0853-20Selected

250 TABLET in 1 BOTTLE (68462-853-20)