NDC 84549-775
Cleocin Phosphate 150 mg per 1 mL injection, solution
On the label: ProPharma Distribution. It's repackaged: ProPharma Distribution rebottles it from Pharmacia & Upjohn Company LLC's NDC 0009-0775.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
Repackaging site
- ProPharma Distribution, Westminster, CO, United States · repackages it and relabels it
Recalls
- Mar 15, 2019 · Class III · Pfizer Inc.
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Lots: Lot #: T97469, Exp. 7/2019, W28574, Exp.09/2019 - Mar 15, 2019 · Class III · Pfizer Inc.
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Lots: Lot#: T78191, Exp.04/2019, T97494, Exp.07/2019 - Mar 15, 2019 · Class III · Pfizer Inc.
Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point
Lots: Lot #: T78193, Exp.04/2019 - Jun 4, 2013 · Class II · Pharmacia & Upjohn LLC
Presence of Particulate Matter: Firm is recalling a small number of vials with very small reflective flakes consistent with delamination of the glass vial.
Lots: Lots: a) G34908, Exp 06/14; G53479, Exp 09/14; G63442, G58347, Exp 10/14; G80133, Exp 12/14; and b) G34910, Exp 06/14; G36879, G41005, Exp 07/14; G53478, Exp 09/14; G63444, Exp 10/14; G76317, Exp 11/14.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Clindamycin: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 150 mg per 1 mL
- Approval
- NDA NDA050441
- On the market since
- Oct 2, 1972
- Package NDCs
84549-775-26- Official label
- DailyMed (National Library of Medicine), updated Jul 18, 2025
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