Home NDC 21130-404 Acid Reducer 150
Product NDC 21130-404
11-digit product format 211300404
Labeler code 21130
Product ID 21130-404_4387adce-20bf-fcdb-62b2-bb17673cf324
Type HUMAN OTC DRUG
Nonproprietary name Ranitidine Hydrochloride Tablets 150mg
Dosage form TABLET, COATED
Route ORAL
Labeler Safeway Inc
Application ANDA078192
Marketing category ANDA
Marketing start 2012-05-14
Marketing end 0000-00-00
Substance RANITIDINE HYDROCHLORIDE
Active strength 150 mg/1
NDC exclude flag No
Listing certified through 2020-12-31
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 · 45 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 21130-404-50 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 21130-404-02 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 21130-404-34 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 21130-404-50 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 21130-404-02 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 21130-404-34 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 21130-404-02 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 21130-404-34 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 21130-404-50 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 21130-404-02 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 21130-404-34 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 21130-404-50 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 21130-404-02 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 21130-404-34 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 21130-404-50 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 21130-404-02 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 21130-404-34 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 21130-404-50 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 21130-404-02 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 21130-404-34 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 21130-404-50 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 21130-404-02 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 21130-404-34 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 21130-404-50 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 21130-404-02 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 21130-404-34 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 21130-404-50 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 21130-404-02 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 21130-404-34 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 21130-404-50 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 21130-404-02 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 21130-404-34 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 21130-404-50 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 21130-404-02 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 21130-404-34 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 21130-404-50 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A078192-001 RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31
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 2 · 42 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 2026-08-18 06:07:40 2026-07 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 782e0a99824c…2021-05-05 16:15 UTC · 3 captures of this ZIP 2021-05 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 87673890dc5c…2021-03-12 10:30 UTC 2021-03 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 5aa47cf7b7d7…2020-12-22 03:56 UTC 2020-12 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 8869cabd3fbd…2020-11-12 02:37 UTC 2020-11 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 c0c555d07b60…2019-12-14 00:12 UTC 2019-12 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 3f01610625f2…2019-09-15 20:21 UTC 2019-09 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 b00525d2431f…2019-07-19 19:46 UTC 2019-07 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 ea99ee380514…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 9b2671bbb829…2023-07-15 15:27 UTC · 2 captures of this ZIP 2023-07 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 a67488948f0b…2023-06-13 01:57 UTC · 3 captures of this ZIP 2023-06 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 3f0d92c62455…2023-05-13 08:27 UTC 2023-05 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 053a50430f4f…2023-01-26 05:58 UTC 2023-01 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 3bdfa0b2c4d7…2022-11-12 20:34 UTC · 5 captures of this ZIP 2022-11 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 3a93d1ddd44b…2022-10-28 04:53 UTC 2022-10 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A078192-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 2007-08-31 e64feba35796…
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded RANITIDINE HYDROCHLORIDE ACTIVE INGREDIENT BK76465IHM ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1 RANITIDINE ACTIVE MOIETY 884KT10YB7 ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1 cellulose, microcrystalline INACTIVE INGREDIENT OP1R32D61U ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1 FERROSOFERRIC OXIDE INACTIVE INGREDIENT XM0M87F357 ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1 HYPROMELLOSE 2910 (6 MPA.S) INACTIVE INGREDIENT 0WZ8WG20P6 ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1 magnesium stearate INACTIVE INGREDIENT 70097M6I30 ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1 titanium dioxide INACTIVE INGREDIENT 15FIX9V2JP ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-404 ACID REDUCER 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [SAFEWAY INC] 3 Legacy NDC 20231103_e6fef940-cc58-abf6-e475-37782d6c835f.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 21130-404-02 21130040402 1 BOTTLE in 1 CARTON (21130-404-02) > 200 TABLET, COATED in 1 BOTTLE 1 bottle 2012-05-14 0000-00-00 No No Current 21130-404-34 21130040434 1 BOTTLE in 1 CARTON (21130-404-34) > 24 TABLET, COATED in 1 BOTTLE 1 bottle 2012-05-14 0000-00-00 No No Current 21130-404-50 21130040450 1 BOTTLE in 1 CARTON (21130-404-50) > 50 TABLET, COATED in 1 BOTTLE 1 bottle 2012-05-14 0000-00-00 No No Current