Ranitidine

Product NDC: 63629-1671
Requested package NDC: 63629-1671-0
11-digit product format: 636291671
Labeler code: 63629
Product ID: 63629-1671_f6e452aa-9fa6-4dbd-b4f7-072f2833c1ae
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Ranitidine
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA077824
Marketing category: ANDA
Marketing start: 2009-12-16
Marketing end: 0000-00-00
Substance: RANITIDINE HYDROCHLORIDE
Active strength: 150 mg/1
Pharmacologic classes: Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	63629-1671	63629-1671-0	D	Discontinued by firm		2026-08-17

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 · 13 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2020-06-10 20:45 UTC · source 2020-06-10	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`

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
A077824-001	RANITIDINE HYDROCHLORIDE	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13
A077824-002	RANITIDINE HYDROCHLORIDE	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13

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	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	AB		2006-10-13	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL	AB	RS	2006-10-13	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A077824-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2006-10-13	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	A077824-002	RANITIDINE HYDROCHLORIDE	EQ 300MG BASE	TABLET / ORAL			2006-10-13	`bb7c543d1eb4…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-13 00:20 UTC	2019-12	A077824-001	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	A077824-002	AB	1	`74a2ff9319b5…`
2019-12-14 00:12 UTC	2019-12	A077824-001	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	A077824-002	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A077824-001	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	A077824-002	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A077824-001	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	A077824-002	AB	1	`ea99ee380514…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
63629-1671-0	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-1	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-2	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-3	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-4	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-5	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-6	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-7	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-8	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-9	2020-06-20	Ranitidine Tablets, USP Rx Only
63629-1671-0	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-1	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-2	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-3	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-4	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-5	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-6	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-7	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-8	2020-01-31	Ranitidine Tablets, USP Rx Only
63629-1671-9	2020-01-31	Ranitidine Tablets, USP Rx Only

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63629-1671-1	EA - Each	63629-1671	9113af36-c2ff-4bef-a384-3cb78803832f	1	2012-07-24
63629-1671-2	EA - Each	63629-1671	514ba796-3433-44dc-adc0-6c50bfb988e1	1	2012-07-24
63629-1671-3	EA - Each	63629-1671	29955b09-961c-4cf3-9969-7c504ec96ffd	1	2012-07-24
63629-1671-4	EA - Each	63629-1671	f48ec7a9-76ee-474d-bc46-08bbb55f6920	1	2012-07-24
63629-1671-5	EA - Each	63629-1671	ac7e964c-5b6f-48a9-8575-0d48ff8fdb8e	1	2012-07-24
63629-1671-6	EA - Each	63629-1671	793c8d14-d467-408e-8962-a1bbc0a1d2fb	1	2015-02-02
63629-1671-7	EA - Each	63629-1671	74deb82d-4dab-4174-8fd4-d7e44666ffe0	1	2015-02-02
63629-1671-8	EA - Each	63629-1671	3c34d228-3e3d-48db-9c4a-a16ff96a8a34	1	2015-02-02
63629-1671-9	EA - Each	63629-1671	e5ab86dc-b4ad-420b-a423-11ef7231f99f	1	2015-02-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
RANITIDINE HYDROCHLORIDE	ACTIVE INGREDIENT	BK76465IHM	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
RANITIDINE	ACTIVE MOIETY	884KT10YB7	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
COLLOIDAL SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
POLYDEXTROSE	INACTIVE INGREDIENT	VH2XOU12IE	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	RANITIDINE TABLET [BRYANT RANCH PREPACK]	2

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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ranitidine	RANITIDINE	Amneal Pharmaceuticals of New York LLC	b38a3332-5c54-453f-aeb7-070f830955c2	2026-05-01	Adverse reactions	Exact identifier application applno (ANDA): 077824 application number: ANDA077824

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
BK76465IHM	RANITIDINE HYDROCHLORIDE	66357-59-3	RANITIDINE HYDROCHLORIDE
884KT10YB7	RANITIDINE	66357-35-5	Ranitidine

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-1671-0	63629167100	10 TABLET in 1 BOTTLE (63629-1671-0)	10 tablet	2009-12-16	0000-00-00	No	No	Current