NDC 69452-126

Sevelamer Carbonate 800 mg powder, for suspension

On the label: Bionpharma Inc..

Switzerland: 1United States: 1India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Alpex Pharma SAMezzovico, SwitzerlandMakes it Problems found, fixed voluntarilyDec 14, 2023 · 3 inspections
Appco Pharma LLCPiscataway, NJ, United StatesMakes it Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections
OrBion Pharmaceuticals Private LimitedKancheepuram, IndiaMakes it No problems foundOct 27, 2025 · 6 inspections

Product details

Generic drug
Sevelamer: every company that makes it
Form
powder, for suspension, oral
Strength
800 mg
Approval
ANDA ANDA209374
On the market since
Sep 1, 2021
Package NDCs
69452-126-19 69452-126-60
Official label
DailyMed (National Library of Medicine), updated Aug 22, 2024

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