Home NDC 71205-635 Quinapril
Product NDC 71205-635
11-digit product format 712050635
Labeler code 71205
Product ID 71205-635_91c30b32-c939-4f18-aa77-1f41d68a29e2
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Quinapril
Dosage form TABLET
Route ORAL
Labeler Proficient Rx LP
Application ANDA077690
Marketing category ANDA
Marketing start 2007-02-26
Substance QUINAPRIL HYDROCHLORIDE
Active strength 10 mg/1
Pharmacologic classes Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 4 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A077690-001 QUINAPRIL HYDROCHLORIDE QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 A077690-002 QUINAPRIL HYDROCHLORIDE QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 A077690-003 QUINAPRIL HYDROCHLORIDE QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 A077690-004 QUINAPRIL HYDROCHLORIDE QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 4 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 1 of 5 · 164 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-02-19 14:30 UTC 2026-02 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A077690-001 QUINAPRIL HYDROCHLORIDE EQ 5MG BASE TABLET / ORAL AB 2006-06-20 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A077690-002 QUINAPRIL HYDROCHLORIDE EQ 10MG BASE TABLET / ORAL AB 2006-06-20 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A077690-003 QUINAPRIL HYDROCHLORIDE EQ 20MG BASE TABLET / ORAL AB 2006-06-20 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A077690-004 QUINAPRIL HYDROCHLORIDE EQ 40MG BASE TABLET / ORAL AB RS 2006-06-20 d06236e962d9…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 5 · 164 observed states.
Additional Listing Data#
Finished product Yes
Brand name base Quinapril
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength QUINAPRIL HYDROCHLORIDE 10 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 33067B3N2M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 312748 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71205-635-30 Quinapril 30 in 1 BOTTLE TABLET 30 2 71205-635-60 Quinapril 60 in 1 BOTTLE TABLET 60 2 71205-635-90 Quinapril 90 in 1 BOTTLE TABLET 90 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71205-635 QUINAPRIL TABLET [PROFICIENT RX LP] 2 Current NDC, Legacy NDC, 3 package rows 20220602_2efb2ede-a49b-4e3e-9c93-4c202f67211f.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 5 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Quinapril QUINAPRIL Northwind Health Company, LLC da562e3b-4411-e750-e053-2a95a90ad7e5 2026-01-01 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077690 application number: ANDA077690 Quinapril QUINAPRIL Bryant Ranch Prepack a6cf2ffd-cf94-4f1c-a12e-ce0e93a6304d 2024-05-20 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077690 application number: ANDA077690 Quinapril QUINAPRIL Lupin Pharmaceuticals, Inc. 8ded0773-3aec-4e89-9836-d22a5a84abf0 2023-12-14 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077690 application number: ANDA077690 Quinapril QUINAPRIL Proficient Rx LP 2efb2ede-a49b-4e3e-9c93-4c202f67211f 2022-05-01 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077690 application number: ANDA077690 ndc (product): 71205-635 Quinapril QUINAPRIL BluePoint Laboratories 1b5809a8-873d-44cb-af59-e0d8fc81b385 2020-08-26 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077690 application number: ANDA077690
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71205-635-30 71205063530 30 TABLET in 1 BOTTLE (71205-635-30) 30 tablet 2022-01-31 0000-00-00 No No Current 71205-635-60 71205063560 60 TABLET in 1 BOTTLE (71205-635-60) 60 tablet 2022-01-31 0000-00-00 No No Current 71205-635-90 71205063590 90 TABLET in 1 BOTTLE (71205-635-90) 90 tablet 2022-01-31 0000-00-00 No No Current