Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Recalls
- Nov 4, 2015 · Class III · Dr. Reddy's Laboratories, Inc.
Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.
Lots: Lot #s: C404795, C404796, C404797, Exp 05/2016; C406272, C406273, C406274, C406518, Exp 07/2016; C409586, C409587, Exp 11/2016; C409588, Exp 12/2016; C501835, C501836 , C501837, Exp 02/2017; C503797, C503798, Exp 05/2017; C505009, Exp 06/2017; C505568, C505569, Exp 07/2017 - Nov 4, 2015 · Class III · Dr. Reddy's Laboratories, Inc.
Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.
Lots: Lot #s: C404653, C404654, C404655, Exp 05/2016; C505010, Exp 06/2017 - Nov 4, 2015 · Class III · Dr. Reddy's Laboratories, Inc.
Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.
Lots: Lot #s: C404440, Exp 04/2016; C404946, Exp 05/2016; C505704, Exp 07/2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Paricalcitol: every company that makes it
- Form
- capsule, liquid filled, oral
- Strength
- 4 ug
- Approval
- ANDA ANDA091412
- On the market since
- Jun 25, 2014
- Package NDCs
55111-665-0155111-665-0555111-665-3055111-665-7955111-665-81- Official label
- DailyMed (National Library of Medicine), updated Apr 27, 2017
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