Albutein
Albumin (human) · Injection, Solution · Intravenous
No FDA structured label text is available for Albutein. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Albumin Human in 5 products
Albutein NDC products (5)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 68516-5214 | Albumin Human 12.5 g/250mL Injection, Solution | GRIFOLS USA, LLC | BLA |
| 68516-5215 | Albumin Human 10 g/50mL Injection, Solution | GRIFOLS USA, LLC | BLA |
| 68516-5216 | Albumin Human 12.5 g/50mL Injection, Solution | GRIFOLS USA, LLC | BLA |
| 68516-5218 | Albumin Human 12.5 g/250mL Injection, Solution | GRIFOLS USA, LLC | BLA |
| 68516-5219 | Albumin Human 12.5 g/250mL Injection, Solution | GRIFOLS USA, LLC | BLA |
Frequently asked questions
Who makes Albutein?
Albutein is listed by 1 labeler in the FDA NDC directory, including GRIFOLS USA, LLC.