NDC 43598-478
Sevelamer Carbonate for Oral Suspension 800 mg powder, for suspension
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Srikakulam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 20, 2022 · 5 inspections |
Recalls
- Jun 26, 2024 · Class III · Dr. Reddy's Laboratories, Inc.
Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets
Lots: Lot #: T2305999, Exp. Date 11/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sevelamer: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA210464
- On the market since
- Oct 25, 2018
- Package NDCs
43598-478-0143598-478-90- Official label
- DailyMed (National Library of Medicine), updated May 20, 2020
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