Quick answers
- What is Acticlate CAP?
- Acticlate CAP is a brand name of Doxycycline, a prescription medicine. The FDA NDC Directory lists 1 Acticlate CAP product in 1 strength and form.
- Who makes Acticlate CAP?
- Chartwell RX holds the FDA application for Acticlate CAP (NDA208253, approved April 26, 2016).
- Is there a generic or store brand of Acticlate CAP?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Acticlate CAP product, 1 of them generic. Ask your pharmacist whether one is right for you.
- Has Acticlate CAP been recalled?
- No recall linked to Acticlate CAP products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Acticlate CAP is
Each Acticlate CAP 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.
Doxycycline · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| doxycycline hyclate 75 mg capsule (oral) | Acticlate CAP | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Doxycycline →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA208253 | Chartwell RX | April 26, 2016 | 1 |
Companies that list Acticlate CAP
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Acticlate CAP products.
- Aqua Pharmaceuticals1 product
Recalls
No recall linked to Acticlate CAP 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.