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Lisinopril brand names generic information 2026?

See the DrugPatentWatch profile for Lisinopril

Lisinopril (generic)
Class: ACE‑inhibitor (angiotensin‑converting enzyme inhibitor)
Mechanism: Blocks the conversion of angiotensin‑I → angiotensin‑II → ↓vasoconstriction, ↓renin release, ↑bradykinin → vasodilation

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1️⃣ Brand Names (2026)


| Region | Brand name(s) | Notes |
|--------|--------------|-------|
| United States | Prinivil, Zestril (both Merck & Co.) | Still the two most common brand names. |
| Canada | Lisopril | Available in 5 mg, 10 mg, 20 mg tablets. |
| United Kingdom | Lisopril (licensed by Pfizer) | Also sold as “Lisopril 5 mg” or “Lisopril 10 mg.” |
| Australia & New Zealand | Lisopril | 5 mg and 10 mg tablets, plus a 20 mg capsule (for advanced heart failure). |
| Europe (other countries) | Lisopril (some countries), Lisopril (many) | Same 5/10/20 mg strength. |
| India | Lisopril, Lisopren (generic & branded) | Multiple manufacturers, often 5 mg & 10 mg tablets. |
| Middle East & Africa | Lisopril | Usually generic, 5 mg & 10 mg. |

Tip: In many regions “Lisopril” is the sole brand name; the generic is simply lisinopril. Check local drug registries for the exact spelling.

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2️⃣ Generic Information (2026)


| Feature | Detail |
|---------|--------|
| Form | Oral tablet, 5 mg, 10 mg, 20 mg; 20 mg capsule (heart failure). |
| Dosage (Hypertension) | 5 mg once daily → titrate ↑5 mg every 2–4 weeks up to 40 mg/day (max 40 mg). |
| Dosage (Heart Failure) | Start 2.5 mg → ↑2.5 mg q4–7 days to 20 mg/day (often split BID). |
| Dosage (Post‑MI) | 5 mg daily → ↑5 mg q4–7 days to 10 mg. |
| Administration | With or without food, same time daily. |
| Onset | 30–60 min; peak effect 2–4 h. |
| Half‑life | 10 h (active metabolite). |
| Metabolism | Hepatic (CYP2C9). Excreted unchanged renally. |
| Renal Consideration | Reduce dose or discontinue in CrCl <30 mL/min. |
| Pregnancy | Category X – teratogenic; contraindicated in all trimesters. |
| Breastfeeding | Not recommended. |
| Age | Safe in pediatrics 6 y+ (heart failure); not FDA‑approved for hypertension in children <6 y. |
| Weight‑based dosing | No special dosing for obesity/under‑weight. |
| Contraindicated | • Prior angioedema from ACEI
• Bilateral renal artery stenosis
• Pregnancy |

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3️⃣ Key Clinical Points (2026)


| Category | Highlights |
|----------|------------|
| Indications | • Primary hypertension
• Stable chronic heart failure
• Post‑myocardial infarction (reduced EF)
• Diabetic nephropathy (proteinuria control) |
| Monitoring | • Blood pressure & pulse q1–2 weeks after dose change
• Serum potassium & creatinine q4–6 weeks after initiation & dose changes
• Watch for angioedema signs |
| Common Adverse Effects | • Dry cough (≈10–20 %)
• Hyperkalemia (especially with potassium‑sparing diuretics)
• Dizziness/orthostatic hypotension
• Angioedema (rare, but life‑threatening) |
| Rare but Serious | • Severe renal impairment
• Angioedema
• Severe hyperkalemia (≥6.5 mmol/L) |
| Drug Interactions | • Potassium supplements / K‑sparing diuretics (increase hyperkalemia risk)
NSAIDs (reduce ACE‑I efficacy; ↑renal dysfunction)
Digoxin (↓excretion → ↑levels)
Lithium (↑renal retention)
Metformin (↓renal clearance → ↑metformin levels)
Other ACE‑I or ARB (additive effect; avoid concomitant use) |
| Patient Counseling | • Take at same time daily; keep a log of BP
• Report cough or swelling of lips/face/neck promptly
• Do not abruptly stop; taper if necessary
• Avoid excessive salt intake (may increase edema risk) |
| Lifestyle Adjuncts | • Low‑salt diet, weight loss, exercise, limit alcohol, quit smoking |
| Pregnancy Warning | Must stop before conception and maintain until delivery; switch to ARB or other class if needed |

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4️⃣ Economic & Accessibility Snapshot (2026)


| Aspect | Status |
|--------|--------|
| Patent | Expired 2013 (US); generics dominate. |
| Generic Competition | > 30 manufacturers worldwide (Pfizer, Bayer, Sun Pharma, Teva, etc.). |
| Cost (US) | 30‑day supply: <$10 (generic 5 mg) to <$20 (generic 20 mg). |
| Insurance Coverage | Usually “Tier 1” (lowest copay) on most formularies. |
| Access in Low‑Income Countries | WHO essential‑medicines list → free‑access in many public health systems; generic supply is robust. |

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5️⃣ Quick Reference Sheet


| Item | 5 mg | 10 mg | 20 mg |
|------|------|-------|-------|
| **



Other Questions About Lisinopril :

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AI-Drug Label Prescribing Information Alignment Report

60
60%
Grade C

Partial

Partially Aligned

Patient Risk: Low

Summary

The claim is broadly consistent with the provided boxed warning/fetal toxicity label excerpts, but the audit content includes non-verifiable/placeholder verification logic and does not clearly demonstrate traceability to exact FDA label wording beyond generic references.


Category Scores

Warnings
70
Good
Warnings
70
Good

Accurate Statements

The boxed warning states that drugs that act directly on the renin-angiotensin system can cause fetal injury and death.
SECTION 1 — WARNING: FETAL TOXICITY (Boxed Warning) and SECTION 5 — Warnings and Precautions: Fetal Toxicity
When pregnancy is detected, discontinue lisinopril and hydrochlorothiazide tablets as soon as possible.
SECTION 1 — WARNING: FETAL TOXICITY (Boxed Warning), SECTION 2 (additional content), and SECTION 8 (pregnancy subsection)

Unsupported Statements

Compliance cannot be confirmed because the response provides only generic section placeholders and does not quote/cite the exact wording from the relevant labeling.
The prompt includes the actual label excerpts for the boxed warning and fetal toxicity section; the issue is about verifiability in the AI response narrative, but it is not an FDA-label content discrepancy. Within the supplied information, the claim is supported.
The verdict is 'cannot_verify_with_provided_info'.
The prompt provides the relevant boxed warning and fetal toxicity wording sufficient to verify that 'WARNING: FETAL TOXICITY' is supported by the label excerpts.

Contradictions

Low

AI Statement
The audit result suggests the claim cannot be verified and therefore implies lack of support.

Label Reference
Supported by the provided FDA label excerpts in SECTION 1 and SECTION 5 (and corroborated by SECTION 2 and SECTION 8).


Important Omissions

The audit output does not clearly reconcile/verifiably map the 'supported' decision to specific quoted elements (e.g., mechanism details and discontinuation instruction) from the provided label excerpts; it instead focuses on generic verifiability rationale.
Importance: Moderate

Safety Assessment

Potential Patient Risk: Low
The content evaluated concerns a boxed warning label alignment; the underlying label excerpts support the warning and discontinuation guidance, so no label-inaccurate safety denial is made.

Regulatory Assessment

On Label Yes
Off-label Discussion No
Promotes Unapproved Use No
Hallucination Risk Low

Recommendation

Partially Aligned

Primary Issue
The audit concludes 'cannot_verify' and cites lack of quoting/citation logic, despite the prompt already containing the relevant FDA label excerpts; this reduces audit alignment/traceability quality.

Suggested Improvement
When the prompt includes the label text, base the verification on the provided excerpts and explicitly tie the decision to the quoted boxed-warning/discontinuation language from SECTION 1/SECTION 5 (and corroborate with SECTION 2/SECTION 8).