Quick answers
- What is Cleocin Pediatric?
- Cleocin Pediatric is a brand name of Clindamycin palmitate hydrochloride, a prescription medicine. The FDA NDC Directory lists 1 Cleocin Pediatric product in 1 strength and form.
- Who makes Cleocin Pediatric?
- Pfizer holds the FDA application for Cleocin Pediatric (ANDA062644, approved April 7, 1986).
- Is there a generic or store brand of Cleocin Pediatric?
- Yes. The FDA NDC Directory lists 5 other products with the same active ingredients, strength and form as a Cleocin Pediatric product, 5 of them generic. Ask your pharmacist whether one is right for you.
- Has Cleocin Pediatric been recalled?
- No recall linked to Cleocin Pediatric products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Cleocin Pediatric is
Each Cleocin Pediatric product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Clindamycin palmitate hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| clindamycin palmitate hydrochloride 75 mg/5 mL granule, for solution (oral) | Cleocin Pediatric | 5 products, 4 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Clindamycin palmitate hydrochloride →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA062644 | Pfizer | April 7, 1986 | 1 |
Companies that list Cleocin Pediatric
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Cleocin Pediatric products.
- Pharmacia & Upjohn Company LLC1 product
Recalls
No recall linked to Cleocin Pediatric products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.