Bleomycin for Injection, USP contains sterile bleomycin sulfate equivalent to 15 units or 30 units of bleomycin.
| Unit of Sale | Concentration |
|---|---|
| NDC 61703-332-18 | 15 units per vial |
| Carton containing 1 single-dose vial | |
| NDC 61703-323-22 | 30 units per vial |
| Carton containing 1 single-dose vial |
Stability
The sterile powder is stable under refrigeration 2°C to 8°C (36°F to 46°F) and should not be used after the expiration date is reached.
Bleomycin for Injection should not be reconstituted or diluted with 5% Dextrose Injection or other dextrose containing diluents. When reconstituted in 5% Dextrose Injection and analyzed by HPLC, Bleomycin for Injection demonstrates a loss of A2 and B2 potency that does not occur when Bleomycin for Injection is reconstituted in Sodium Chloride for Injection, 0.9%, USP.
Bleomycin for Injection, USP is stable for 24 hours at room temperature in Sodium Chloride.
Bleomycin for Injection, USP contains sterile bleomycin sulfate equivalent to 15 units or 30 units of bleomycin.
| Unit of Sale | Concentration |
|---|---|
| NDC 61703-332-18 | 15 units per vial |
| Carton containing 1 single-dose vial | |
| NDC 61703-323-22 | 30 units per vial |
| Carton containing 1 single-dose vial |
Stability
The sterile powder is stable under refrigeration 2°C to 8°C (36°F to 46°F) and should not be used after the expiration date is reached.
Bleomycin for Injection should not be reconstituted or diluted with 5% Dextrose Injection or other dextrose containing diluents. When reconstituted in 5% Dextrose Injection and analyzed by HPLC, Bleomycin for Injection demonstrates a loss of A2 and B2 potency that does not occur when Bleomycin for Injection is reconstituted in Sodium Chloride for Injection, 0.9%, USP.
Bleomycin for Injection, USP is stable for 24 hours at room temperature in Sodium Chloride.
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