Class III ยท Low risk
Tyvaso Inhalation System Patient a) Starter Kit with TYVASO
Defective Delivery System: Water ingress through the lower water cup sensor of the device.
National Drug Code
Is NDC 66302-0206-01 recalled?
Tyvaso · 1 BOX in 1 KIT (66302-206-01) / 28 AMPULE in 1 BOX / 2.9 mL in 1 AMPULE
Yes — this exact package was recalled
1 FDA recall names the code 66302-0206-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- treprostinil
- Strength
- TREPROSTINIL 1.74 mg/2.9mL
- Form
- Inhalant · Oral
- Labeler
- United Therapeutics Corporation
- Type
- Human Prescription Drug
- Product code
- 66302-0206
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 66302-2060 See recall 1
Free recall alerts
Know the day your medication is recalled
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