FDA NDC Directory · JSON-LD · Markdown

PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID

NDC 0093-3560 · HUMAN PRESCRIPTION DRUG · KIT

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090145
Dosage form / routeKIT
Active ingredients—
Marketing started20200831
Package count1

External sources

Source: openFDA. Public-domain (CC0).