Diluent
Injection · Subcutaneous, Intravenous
No FDA structured label text is available for Diluent. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Water in 1 product
- Sodium Chloride in 1 product
- Carboxymethylcellulose Sodium in 1 product
Diluent NDC products (3)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 0781-6021 | Water 1 mL/mL Injection | Sandoz Inc | ANDA |
| 49281-912 | Sodium Chloride 4.5 mg/.5mL Injection | Sanofi Vaccines US Inc. | BLA |
| 61434-011 | Carboxymethylcellulose Sodium 25 mg/5mL Solution | Catalent Indiana, LLC | DRUG FOR FURTHER PROCESSING |
Frequently asked questions
Who makes Diluent?
Diluent is listed by 3 labelers in the FDA NDC directory, including Sandoz Inc, Sanofi Vaccines US Inc., Catalent Indiana, LLC.