Quick answers
- What is Orphengesic Forte?
- Orphengesic Forte is a brand name of Orphenadrine citrate, aspirin and caffeine, a prescription medicine. The FDA NDC Directory lists 1 Orphengesic Forte product in 1 strength and form.
- Who makes Orphengesic Forte?
- Galt Pharms holds the FDA application for Orphengesic Forte (ANDA075141, approved May 29, 1998).
- Is there a generic or store brand of Orphengesic Forte?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Orphengesic Forte product, 1 of them generic. Ask your pharmacist whether one is right for you.
- Has Orphengesic Forte been recalled?
- No recall linked to Orphengesic Forte products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Orphengesic Forte is
Each Orphengesic Forte 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.
Orphenadrine citrate, aspirin and caffeine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| aspirin 770 mg · caffeine 60 mg · orphenadrine citrate 50 mg tablet (oral) | Orphengesic Forte | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Orphenadrine citrate, aspirin and caffeine →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA075141 | Galt Pharms | May 29, 1998 | 1 |
Companies that list Orphengesic Forte
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Orphengesic Forte products.
- Galt Pharmaceuticals, LLC1 product
Recalls
No recall linked to Orphengesic Forte 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.