NDC 70710-2180 – Sodium phenylbutyrate

Sodium Phenylbutyrate 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70710-2180

Product details

Brand name
Sodium phenylbutyrate
Generic name
Sodium phenylbutyrate
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA220418
Marketed since
March 23, 2026
Listing expires
December 31, 2027
Pharmacologic class
Nitrogen Binding Agent

Active ingredients

Uses, dosage, side effects and warnings for sodium phenylbutyrate →

Package NDC codes (1)

Package NDCDescriptionSince
70710-2180-81 BOTTLE in 1 CARTON (70710-2180-8) / 250 TABLET in 1 BOTTLEMar 23, 2026

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