Quick answers
- What is ConZip?
- ConZip is a brand name of Tramadol hydrochloride, a prescription medicine. The FDA NDC Directory lists 3 ConZip products in 3 strengths and forms.
- Who makes ConZip?
- Cipher Pharms Inc holds the FDA application for ConZip (NDA022370, approved May 7, 2010).
- Is there a generic or store brand of ConZip?
- Other products of Tramadol hydrochloride are listed with the FDA, but none in exactly the same strength and form as a ConZip product.
- Has ConZip been recalled?
- No recall linked to ConZip products (by their NDC code or label) appears in the FDA enforcement reports we use.
What ConZip is
Each ConZip 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.
Tramadol hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| tramadol hydrochloride 100 mg capsule, extended release (oral) | ConZip | None listed | DailyMed |
| tramadol hydrochloride 200 mg capsule, extended release (oral) | ConZip | None listed | DailyMed |
| tramadol hydrochloride 300 mg capsule, extended release (oral) | ConZip | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Tramadol hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA022370 | Cipher Pharms Inc | May 7, 2010 | 3 |
Companies that list ConZip
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of ConZip products.
- Vertical Pharmaceuticals, LLC3 products
Recalls
No recall linked to ConZip 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.