Home NDC 50090-2977 Fosinopril Sodium
Product NDC 50090-2977
11-digit product format 500902977
Labeler code 50090
Product ID 50090-2977_8f99a421-7303-41b5-bde9-f9beb408fcf8
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Fosinopril
Dosage form TABLET
Route ORAL
Labeler A-S Medication Solutions
Application ANDA077222
Marketing category ANDA
Marketing start 2016-06-16
Substance FOSINOPRIL SODIUM
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 50090-2977 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 50090-2977 50090-2977-0 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A077222-001 FOSINOPRIL SODIUM FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 A077222-002 FOSINOPRIL SODIUM FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 A077222-003 FOSINOPRIL SODIUM FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 3 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 4 · 129 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 2026-09-14 22:38:34 2026-08 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 84e616aacf4f…2026-09-14 22:38:34 2026-08 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 84e616aacf4f…2026-09-14 22:38:34 2026-08 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 84e616aacf4f…2026-08-18 06:07:40 2026-07 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A077222-002 FOSINOPRIL SODIUM 20MG TABLET / ORAL AB 2005-04-20 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A077222-003 FOSINOPRIL SODIUM 40MG TABLET / ORAL AB 2005-04-20 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A077222-001 FOSINOPRIL SODIUM 10MG TABLET / ORAL AB 2005-04-20 301d65b070ca…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 4 · 129 observed states.
Additional Listing Data#
Finished product Yes
Brand name base Fosinopril Sodium
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FOSINOPRIL SODIUM 10 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination NW2RTH6T2N Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 857169 Internal RxNorm lookup 857187 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50090-2977-0 Fosinopril Sodium 30 in 1 BOTTLE TABLET 30 19
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50090-2977 FOSINOPRIL SODIUM (FOSINOPRIL) TABLET [A-S MEDICATION SOLUTIONS] 19 Current NDC, Legacy NDC, 1 package rows 20230219_880e5bf4-ced8-4765-a5c2-2361fd06ed9c.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 Fosinopril Sodium FOSINOPRIL Bryant Ranch Prepack fc38f1bb-f175-4a81-8ed9-c8701efdea35 2023-11-27 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077222 application number: ANDA077222 Fosinopril Sodium FOSINOPRIL Bryant Ranch Prepack 6562a532-b502-4515-88df-591d71293b56 2023-10-19 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077222 application number: ANDA077222 Fosinopril sodium FOSINOPRIL SODIUM Exelan Pharmaceuticals, Inc. e2ff3171-a17a-456a-9272-ca1682b01d19 2023-03-23 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077222 application number: ANDA077222 Fosinopril Sodium FOSINOPRIL A-S Medication Solutions 880e5bf4-ced8-4765-a5c2-2361fd06ed9c 2023-02-17 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077222 application number: ANDA077222 ndc (product): 50090-2977 Fosinopril Sodium FOSINOPRIL Cipla USA Inc. 736fe52f-69fb-48b2-b1c5-f06531878538 2023-01-20 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 077222 application number: ANDA077222
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 50090-2977-0 50090297700 30 TABLET in 1 BOTTLE (50090-2977-0) 30 tablet 2017-04-18 No No Current