Home NDC 30142-505-34 Heratburn Relief
Product NDC 30142-505
Requested package NDC 30142-505-34
11-digit product format 301420505
Labeler code 30142
Product ID 30142-505_d6e047f7-2741-7dd6-d18c-ae738cd70f0e
Type HUMAN OTC DRUG
Nonproprietary name Ranitidine
Dosage form TABLET, COATED
Route ORAL
Labeler The Kroger Co.
Application ANDA078192
Marketing category ANDA
Marketing start 2011-04-24
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 · 12 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…
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 HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1 RANITIDINE ACTIVE MOIETY 884KT10YB7 HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1 cellulose, microcrystalline INACTIVE INGREDIENT OP1R32D61U HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1 FERROSOFERRIC OXIDE INACTIVE INGREDIENT XM0M87F357 HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1 HYPROMELLOSE 2910 (6 MPA.S) INACTIVE INGREDIENT 0WZ8WG20P6 HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1 magnesium stearate INACTIVE INGREDIENT 70097M6I30 HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1 titanium dioxide INACTIVE INGREDIENT 15FIX9V2JP HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 30142-505 HERATBURN RELIEF (RANITIDINE) TABLET, COATED [THE KROGER CO.] 3 Legacy NDC 20231103_2e205ac8-2008-b4b8-021c-61e660781be6.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 30142-505-34 30142050534 1 BOTTLE in 1 CARTON (30142-505-34) > 24 TABLET, COATED in 1 BOTTLE 1 bottle 2011-04-24 0000-00-00 No No Current