Qelbree
viloxazine hydrochloride · Capsule, Extended Release · Oral
No FDA structured label text is available for Qelbree. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Viloxazine Hydrochloride in 3 products
Qelbree NDC products (3)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 17772-131 | Viloxazine Hydrochloride 100 mg/1 Capsule, Extended Release | Supernus Pharmaceuticals, Inc | NDA |
| 17772-132 | Viloxazine Hydrochloride 150 mg/1 Capsule, Extended Release | Supernus Pharmaceuticals, Inc | NDA |
| 17772-133 | Viloxazine Hydrochloride 200 mg/1 Capsule, Extended Release | Supernus Pharmaceuticals, Inc | NDA |
Frequently asked questions
Who makes Qelbree?
Qelbree is listed by 1 labeler in the FDA NDC directory, including Supernus Pharmaceuticals, Inc.