Home NDC 62135-967 Moexipril Hydrochloride
Product NDC 62135-967
11-digit product format 621350967
Labeler code 62135
Product ID 62135-967_3001c14d-1545-86fb-e063-6294a90a035f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Moexipril Hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Chartwell RX, LLC
Application ANDA077536
Marketing category ANDA
Marketing start 2006-11-30
Substance MOEXIPRIL HYDROCHLORIDE
Active strength 7.5 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 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A077536-001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 A077536-002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 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 3 · 82 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 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 8072bd15b7f6…2024-05-31 18:47 UTC 2024-05 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 5c6f7cd8ea54…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 5d02ea3f76ae…2022-04-08 23:34 UTC 2022-04 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 4b0b4de00fa7…2022-04-04 05:41 UTC 2022-04 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 74a2ff9319b5…2019-12-13 00:20 UTC 2019-12 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 bb7c543d1eb4…2022-03-09 01:35 UTC 2022-03 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A077536-001 MOEXIPRIL HYDROCHLORIDE 7.5MG TABLET / ORAL AB 2006-11-30 782e0a99824c…2021-12-28 21:50 UTC 2021-12 A077536-002 MOEXIPRIL HYDROCHLORIDE 15MG TABLET / ORAL AB 2006-11-30 782e0a99824c…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 82 observed states.
Additional Listing Data#
Finished product Yes
Brand name base Moexipril Hydrochloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MOEXIPRIL HYDROCHLORIDE 7.5 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination Q1UMG3UH45 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1299896 Internal RxNorm lookup 1299897 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 62135-967-90 Moexipril Hydrochloride 90 in 1 BOTTLE TABLET, FILM COATED 90 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62135-967 MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CHARTWELL RX, LLC] 1 Current NDC, 1 package rows 20250312_5c24072c-9769-4cb5-b8da-bf814d21391d.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 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 62135-967-90 62135096790 90 TABLET, FILM COATED in 1 BOTTLE (62135-967-90) 2025-03-05 No No Current