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Lisinopril

NDC 65862-039 · Aurobindo Pharma Limited

Generic nameLisinopril
Dosage formTABLET
RouteORAL
Active ingredient(s)LISINOPRIL
Strength10 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
Marketing categoryANDA

Packages

65862-039-00 — 100 TABLET in 1 BOTTLE (65862-039-00)

65862-039-01 — 100 TABLET in 1 BOTTLE (65862-039-01)

65862-039-05 — 500 TABLET in 1 BOTTLE (65862-039-05)

65862-039-30 — 30 TABLET in 1 BOTTLE (65862-039-30)

65862-039-99 — 1000 TABLET in 1 BOTTLE (65862-039-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-825 — Lisinopril, 63629-1761 — Lisinopril, 63629-3739 — Lisinopril and Hydrochlorothiazide, 63629-4470 — Lisinopril and Hydrochlorothiazide, 63629-5247 — Lisinopril, 63629-5382 — Lisinopril, 63629-8736 — Lisinopril, 63629-8823 — Lisinopril, 65862-037 — Lisinopril, 65862-038 — Lisinopril, 65862-040 — Lisinopril, 65862-041 — Lisinopril, 65862-042 — Lisinopril, 65862-043 — Lisinopril and Hydrochlorothiazide, 65862-044 — Lisinopril and Hydrochlorothiazide, 65862-045 — Lisinopril and Hydrochlorothiazide, 67046-0422 — Lisinopril, 67046-0423 — Lisinopril, 67046-0433 — Lisinopril and Hydrochlorothiazide, 67046-0858 — Lisinopril, +342 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.