Quinapril Hydrochloride Tablet
Brand names: Quinapril
Category: Cardiovascular
FDA status: Current, To Be Discontinued · Last FDA update: Oct 1, 2025 · First posted: Jan 19, 2023 (in shortage 3 years 8 months) · 5 manufacturers, 19 listed presentations
As of Oct 1, 2025, the FDA lists Quinapril Hydrochloride Tablet as being discontinued. Of 19 manufacturer presentations, 11 Unavailable, 4 Available, 4 Not specified.
| Presentation & package NDC | Manufacturer | Availability | FDA note |
|---|---|---|---|
| Quinapril Hydrochloride, Tablet, 5 mg (NDC 65862-617-90) NDC 65862-617-90 |
Aurobindo Pharma USA | Unavailable | Discontinuation of the manufacture of the drug |
| Quinapril Hydrochloride, Tablet, 5 mg (NDC 68180-556-09) NDC 68180-556-09 |
Lupin Pharmaceuticals, Inc. | Unavailable | Estimated recovery: TBD |
| Quinapril Hydrochloride, Tablet, 5 mg (NDC 43547-410-09) NDC 43547-410-09 |
Solco Healthcare US, LLC | Unavailable | Not available. Long-term backorder for all NDCs. No estimated release date at this time. |
| Quinapril Hydrochloride, Tablet, 5 mg (NDC 62135-484-60) NDC 62135-484-60 |
Chartwell Molecular Holdings LLC | Available | - |
| Accupril, Tablet, 5 mg (NDC 0071-0527-23) NDC 0071-0527-23 |
Pfizer Inc. | Not specified | Discontinuation of the manufacture of the drug |
| Quinapril Hydrochloride, Tablet, 10 mg (NDC 65862-618-90) NDC 65862-618-90 |
Aurobindo Pharma USA | Unavailable | Discontinuation of the manufacture of the drug |
| Quinapril Hydrochloride, Tablet, 10 mg (NDC 68180-557-09) NDC 68180-557-09 |
Lupin Pharmaceuticals, Inc. | Unavailable | Estimated recovery: TBD |
| Quinapril Hydrochloride, Tablet, 10 mg (NDC 43547-411-09) NDC 43547-411-09 |
Solco Healthcare US, LLC | Unavailable | Not available. Long-term backorder for all NDCs. No estimated release date at this time. |
| Quinapril Hydrochloride, Tablet, 10 mg (NDC 62135-485-90) NDC 62135-485-90 |
Chartwell Molecular Holdings LLC | Available | - |
| Accupril, Tablet, 10 mg (NDC 0071-0530-23) NDC 0071-0530-23 |
Pfizer Inc. | Not specified | Discontinuation of the manufacture of the drug |
| Quinapril Hydrochloride, Tablet, 20 mg (NDC 68180-558-09) NDC 68180-558-09 |
Lupin Pharmaceuticals, Inc. | Unavailable | Estimated recovery: TBD |
| Quinapril Hydrochloride, Tablet, 20 mg (NDC 43547-412-09) NDC 43547-412-09 |
Solco Healthcare US, LLC | Unavailable | Not available. Long-term backorder for all NDCs. No estimated release date at this time. |
| Quinapril Hydrochloride, Tablet, 20 mg (NDC 62135-486-90) NDC 62135-486-90 |
Chartwell Molecular Holdings LLC | Available | - |
| Accupril, Tablet, 20 mg (NDC 0071-0532-23) NDC 0071-0532-23 |
Pfizer Inc. | Not specified | Discontinuation of the manufacture of the drug |
| Quinapril Hydrochloride, Tablet, 40 mg (NDC 65862-620-90) NDC 65862-620-90 |
Aurobindo Pharma USA | Unavailable | Discontinuation of the manufacture of the drug |
| Quinapril Hydrochloride, Tablet, 40 mg (NDC 68180-554-09) NDC 68180-554-09 |
Lupin Pharmaceuticals, Inc. | Unavailable | Estimated recovery: TBD |
| Quinapril Hydrochloride, Tablet, 40 mg (NDC 43547-413-09) NDC 43547-413-09 |
Solco Healthcare US, LLC | Unavailable | Not available. Long-term backorder for all NDCs. No estimated release date at this time. |
| Quinapril Hydrochloride, Tablet, 40 mg (NDC 62135-487-90) NDC 62135-487-90 |
Chartwell Molecular Holdings LLC | Available | - |
| Accupril, Tablet, 40 mg (NDC 0071-0535-23) NDC 0071-0535-23 |
Pfizer Inc. | Not specified | Discontinuation of the manufacture of the drug |
Related medications in shortage
Other Cardiovascular medications currently on the FDA shortage list — useful context if you and your prescriber are weighing alternatives. Always confirm with your pharmacist.
Change log
Tracking began Oct 1, 2026. We check the FDA every 6 hours; any real change - a manufacturer moving from Limited to Available, a new recovery date, a new listing - shows up here with its date.
Cite this: “FDA drug-shortage status for Quinapril Hydrochloride Tablet (FDA data as of Oct 1, 2025). Shortage Watch, openFDA.”
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FDA data last synced Oct 1, 2026 (FDA record dated Sep 30, 2026).