Home NDC 0172-4358 Ranitidine
Product NDC 0172-4358
11-digit product format 001724358
Labeler code 0172
Product ID 0172-4358_e7ffa0e4-b087-4398-977a-57347f89b470
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ranitidine
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Teva Pharmaceuticals USA, Inc.
Application ANDA075165
Marketing category ANDA
Marketing start 1998-04-01
Marketing end 0000-00-00
Substance RANITIDINE HYDROCHLORIDE
Active strength 300 mg/1
Pharmacologic classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
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 · 36 matching rows.
View current auxiliary records. · View the auxiliary file history.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
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 A075165-001 RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 A075165-002 RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30
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 · 84 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 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 8072bd15b7f6…2024-05-31 18:47 UTC 2024-05 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 5c6f7cd8ea54…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 5d02ea3f76ae…2022-04-08 23:34 UTC 2022-04 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 4b0b4de00fa7…2022-04-04 05:41 UTC 2022-04 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL AB 1998-09-30 74a2ff9319b5…2019-12-13 00:20 UTC 2019-12 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL AB 1998-09-30 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A075165-001 RANITIDINE HYDROCHLORIDE EQ 150MG BASE TABLET / ORAL 1998-09-30 bb7c543d1eb4…2022-03-09 01:35 UTC 2022-03 A075165-002 RANITIDINE HYDROCHLORIDE EQ 300MG BASE TABLET / ORAL 1998-09-30 bb7c543d1eb4…
Observed Orange Book normalized TE history# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded RANITIDINE HYDROCHLORIDE ACTIVE INGREDIENT BK76465IHM RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 RANITIDINE ACTIVE MOIETY 884KT10YB7 RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 FERRIC OXIDE RED INACTIVE INGREDIENT 1K09F3G675 RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 FERRIC OXIDE YELLOW INACTIVE INGREDIENT EX438O2MRT RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 LACTOSE MONOHYDRATE INACTIVE INGREDIENT EWQ57Q8I5X RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM RANITIDINE TABLET, FILM COATED [IVAX PHARMACEUTICALS, INC.] 6 RANITIDINE HYDROCHLORIDE ACTIVE INGREDIENT BK76465IHM RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 RANITIDINE ACTIVE MOIETY 884KT10YB7 RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 FERRIC OXIDE RED INACTIVE INGREDIENT 1K09F3G675 RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 FERRIC OXIDE YELLOW INACTIVE INGREDIENT EX438O2MRT RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 LACTOSE MONOHYDRATE INACTIVE INGREDIENT EWQ57Q8I5X RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM RANITIDINE TABLET, FILM COATED [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS] 3