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Amlodipine single-agent tablets - starting dose and renal statement
Product / population
Adults; named product and route only. Selected dosing and renal summary, not the full prescribing information.
Renal method
No renal-function dose bands specified for this summary.
Source revision
Selected repackaged label updated 2022-01-21; prescribing text revised January 2017.
Retrieved
2026-09-05
Local review status
Locally included source-specific summary. Regimen differences are not automatically resolved.
Official
Amlodipine single-agent tablets - starting dose and renal statement
NIH/NLM DailyMed - U.S. product labeling · Adults; named product and route only. Selected dosing and renal summary, not the full prescribing information.
Renal method: No renal-function dose bands specified for this summary. Source date: Selected repackaged label updated 2022-01-21; prescribing text revised January 2017. Retrieved: 2026-09-05
Locally included source-specific summary. Regimen differences are not automatically resolved.
Dosing / renal protocol and limits
Adult hypertension: begin 5 mg orally once daily and titrate to a maximum of 10 mg daily. A 2.5-mg starting dose may be appropriate for small, frail or elderly patients, or hepatic insufficiency. Renal failure alone does not require lowering the usual starting dose. Titrate to blood pressure and tolerability; generally allow 7-14 days between changes. This selected repackaged label has an older revision; current availability of its NDC is not claimed.
RDM30-079-amlodipine-1 · Source locator: Amlodipine single-agent tablets - starting dose and renal statement; renal/dosing sections and stated qualifiers
This reference does not select a regimen. Complete the indication, measured/estimated renal function and trend, dialysis setting, source rationale, monitoring and reassessment plan in your institution's approved documentation system. Confirm the complete current source before adopting its regimen.
GlobalRPh v6.6 | RDM66-DIRECT-PHP-20260911 | Local library date 2026-09-11. Selected-card identity does not imply clinical verification.