Home NDC 50090-2923-0 Atenolol
Product NDC 50090-2923
Requested package NDC 50090-2923-0
11-digit product format 500902923
Labeler code 50090
Product ID 50090-2923_a97585b6-7c97-46fa-999d-f6602babacf0
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Atenolol
Dosage form TABLET
Route ORAL
Labeler A-S Medication Solutions
Application ANDA073025
Marketing category ANDA
Marketing start 1991-09-17
Marketing end 0000-00-00
Substance ATENOLOL
Active strength 50 mg/1
Pharmacologic classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record 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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Source provenance: Browse the complete Orange Book source catalog .
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.
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 2019-12-13 00:20 UTC 2019-12 A073025-001 ATENOLOL 50MG TABLET / ORAL AB 1991-09-17 74a2ff9319b5…2019-12-14 00:12 UTC 2019-12 A073025-001 ATENOLOL 50MG TABLET / ORAL AB 1991-09-17 3f01610625f2…2019-09-15 20:21 UTC 2019-09 A073025-001 ATENOLOL 50MG TABLET / ORAL AB 1991-09-17 b00525d2431f…2019-07-19 19:46 UTC 2019-07 A073025-001 ATENOLOL 50MG TABLET / ORAL AB 1991-09-17 ea99ee380514…
Observed Orange Book normalized TE history# 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 50090-2923-0 Atenolol 100 in 1 BOTTLE TABLET 100 11 50090-2923-7 Atenolol 200 in 1 BOTTLE TABLET 200 11 50090-2923-8 Atenolol 90 in 1 BOTTLE TABLET 90 11
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50090-2923 ATENOLOL TABLET [A-S MEDICATION SOLUTIONS] 11 Legacy NDC, 3 package rows 20200122_e6611d33-f4c7-40c4-8db8-6f43c85d444c.zip
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 50090-2923-0 50090292300 100 TABLET in 1 BOTTLE (50090-2923-0) 100 tablet 2017-03-23 0000-00-00 No No Current