420 695 Pill — WHITE CAPSULE, 19mm — Diltiazem

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Imprint420 / 695
ColourWHITE
ShapeCAPSULE
Size19
StrengthDILTIAZEM HYDROCHLORIDE 420 mg
Dosage formTablet, Extended Release
ManufacturerWatson Pharma, Inc.
NDC62037-695
Schedule—
Availability—
IngredientsDILTIAZEM HYDROCHLORIDE[DILTIAZEM]

What does this imprint mean?

The imprint "420 695" is a code stamped or printed on the tablet or capsule by the manufacturer, used to identify the drug, its strength and the maker.

Active ingredient

Diltiazem

Uses and warnings

No boxed warning. Diltiazem is contraindicated in patients with "sick sinus syndrome except in the presence of a functioning ventricular pacemaker," "second- or third-degree AV block" (without a pacemaker), "hypotension (less than 90 mm Hg systolic)," and acute myocardial infarction with pulmonary congestion documented by X-ray. Key warnings cover cardiac conduction abnormalities, including "second- or third-degree AV block" reported in a small percentage of patients, potential worsening of congestive heart failure in patients with ventricular dysfunction, and symptomatic hypotension.

Diltiazem hydrochloride extended-release capsules are indicated for: - "Treatment of hypertension," alone or in combination with other antihypertensive medications - "Management of chronic stable angina" and "angina due to coronary artery spasm (vasospastic angina)"

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Official references

Source: FDA Structured Product Label via NLM Pillbox archive (retired 2021); source file 0f490ac8-098e-4677-becc-1887794dad21.xml