
NephLong
Annova Plus
Details
500/20 mg
500/20 mg
📌 Generic Composition
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Naproxen sodium – a NSAID (non‑steroidal anti‑inflammatory drug)
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Esomeprazole magnesium – a proton pump inhibitor (PPI)
This combination pairs enteric‑coated naproxen (for pain/inflammation) with an immediate-release layer of esomeprazole (to reduce stomach acid), protecting against NSAID-induced ulcers.
💊 Dosage Forms & Strengths
Available as delayed-release, capsule-shaped, film-coated oral tablets with two strengths:
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375 mg naproxen / 20 mg esomeprazole
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500 mg naproxen / 20 mg esomeprazole
Tablets are biconvex, off-white to yellow, printed with identification codes (“R 289” for 375/20; “R 701” for 500/20).
🧑⚕️ Indications & Dosage
Adults (≥18 years)
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One tablet twice daily, at least 30 minutes before meals:
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375 mg/20 mg or
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500 mg/20 mg naproxen/esomeprazole
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Used for:
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Rheumatoid arthritis
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Osteoarthritis
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Ankylosing spondylitis
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Patients needing NSAID therapy with ulcer risk
Adolescents (12 years & older) with Juvenile Idiopathic Arthritis
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Weight 38–<50 kg: 375 mg/20 mg twice daily
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Weight ≥50 kg: either 375/20 or 500/20 twice daily
⚠️ Administration Notes
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Swallow whole with water at least 30 minutes before meals
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Do not chew, crush, or split the tablet
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If a dose is missed, take ASAP unless the next dose is near — do not double up
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Antacids may be used concurrently
🧩 Product Description
A combination therapy branded as Vimovo in some markets, consisting of an enteric‑coated naproxen core surrounded by an immediate-release esomeprazole layer. This design delays naproxen absorption (reducing acute pain use) while promptly lowering gastric acid to protect the stomach.
📊 Summary Table
| Strength | Naproxen (mg) | Esomeprazole (mg) | Description |
|---|---|---|---|
| 375 mg / 20 mg | 375 | 20 | Film-coated, delayed-release oral tablet |
| 500 mg / 20 mg | 500 | 20 | Same tablet type; higher naproxen dose |
✅ Final Takeaway
Annova Plus is a prescription-only, delayed-release tablet combining naproxen sodium and esomeprazole magnesium. It’s designed for twice-daily use (either 375/20 or 500/20 mg) in adults and appropriate adolescents to treat arthritis symptoms and reduce the risk of NSAID-related gastric ulcers. It must be swallowed whole, 30 minutes before meals, as part of a carefully managed treatment plan under physician guidance.
Keto Nephron™ DS is a Medical Food as defined under 21 U.S.C. §360ee(b)(3) and 21 CFR 101.9(j)(8), formulated for the dietary management of Chronic Kidney Disease (CKD) Stages 3-5 in adults following physician-supervised protein-restricted diets. It is not a drug, not a dietary supplement, and is not intended for self-medication or general wellness use. MUST BE USED UNDER MEDICAL SUPERVISION. Quantum LifeSciences Inc., Claremont, CA 91711, USA. FDA Food Facility (Manufacturer) Reg. No. 14961463490.