up and up famotidine

Product NDC: 11673-031
11-digit product format: 116730031
Labeler code: 11673
Product ID: 11673-031_763d7c0c-950b-42ea-96e1-745e8445bb65
Type: HUMAN OTC DRUG
Nonproprietary name: Famotidine
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Target Corporation
Application: ANDA075400
Marketing category: ANDA
Marketing start: 2015-03-13
Marketing end: 0000-00-00
Substance: FAMOTIDINE
Active strength: 10 mg/1
Pharmacologic classes: Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag: No
Listing certified through: 2023-12-31
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 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	11673-031		D	Discontinued by firm	2026-08-03
excluded package	package	11673-031	11673-031-65	D	Discontinued by firm	2026-08-03
excluded package	package	11673-031	11673-031-72	D	Discontinued by firm	2026-08-03

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 · 8 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11673-031-72	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11673-031-65	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11673-031-65	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	11673-031-65	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	11673-031-65	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	11673-031-65	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	11673-031-65	`cdf11ea48f46…`	`ba0047e9e063…`

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

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
A075400-001	FAMOTIDINE	FAMOTIDINE	10MG	TABLET / ORAL			2005-03-18

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 · 41 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`ea99ee380514…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	A075400-001	FAMOTIDINE	10MG	TABLET / ORAL	2005-03-18	`cb3db0bc1861…`

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
FAMOTIDINE	ACTIVE INGREDIENT	5QZO15J2Z8	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
FAMOTIDINE	ACTIVE MOIETY	5QZO15J2Z8	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
CARNAUBA WAX	INACTIVE INGREDIENT	R12CBM0EIZ	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
POLYDEXTROSE	INACTIVE INGREDIENT	VH2XOU12IE	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET [TARGET CORPORATION]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-031	UP AND UP FAMOTIDINE (FAMOTIDINE) TABLET, FILM COATED [TARGET CORPORATION]	6	Legacy NDC	20250214_0d6f2ac0-295e-47ce-aedb-8cadc1e66a63.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 · 19 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CareOne Acid Relief	FAMOTIDINE	American Sales Company	ed474c9d-c08b-4f52-8b24-5887978e4275	2026-07-01	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
acid relief	FAMOTIDINE	Rite Aid Corporation	9826dd26-5592-4f96-9274-005ef9462cb4	2026-05-27	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
good sense acid reducer	FAMOTIDINE	L. Perrigo Company	cc77f6ff-a534-4731-b971-491280840899	2026-05-18	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
acid reducer original strength	FAMOTIDINE	HyVee Inc	a0f2683f-59ad-4f65-a108-696430d577ab	2026-03-16	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
Acid Controller Original Strength	FAMOTIDINE	Walgreen Company	98c6ddc9-8103-40b3-a145-ffbe3374ab6c	2026-03-03	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
heartburn relief original strength	FAMOTIDINE	Major Pharmaceuticals	be275c48-18bf-45f6-891d-36d89327813e	2026-02-13	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
ACID CONTROLLER	FAMOTIDINE	Safeway	9ddfb9fd-1b84-4e9a-90b5-6a3362d345dd	2025-08-13	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
acid controller	FAMOTIDINE	H E B	813d742f-8f3d-4f18-a6c5-03eea946f976	2025-06-23	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
TopCare Acid Reducer	FAMOTIDINE	Topco Associates LLC	88722f84-dac8-4130-93b3-9e0dc1cc5acc	2025-06-13	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
heartburn relief	FAMOTIDINE	Meijer Distribution Inc	05c03fd8-abc8-47f7-868c-895b9a38c5b3	2025-02-17	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
acid reducer	FAMOTIDINE	Publix Super Markets Inc	a3ba9983-6747-45b2-b270-4ac1fb9d6e40	2025-02-17	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
acid controller original strength	FAMOTIDINE	CVS Pharmacy	c7cb4e19-3442-45d2-b60a-87d4beea862a	2025-02-13	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
dg health heartburn prevention original strength	FAMOTIDINE	Dolgencorp, LLC	f5c0ff75-77da-443c-a510-9c6a065ddc6c	2025-02-11	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
foster and thrive acid reducer	FAMOTIDINE	Strategic Sourcing Services LLC	9ff8539f-cdcd-4823-8baa-10a249c9220d	2025-02-10	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
basic care acid reducer	FAMOTIDINE	Amazon.com Services LLC	52e3b2f5-f3b9-4f4e-a70f-322eb04e6e8a	2025-02-10	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
signature care acid controller	FAMOTIDINE	Safeway	adbf2c58-cd1c-4444-b133-21a18a348931	2025-02-10	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
equaline heartburn prevention	FAMOTIDINE	United Natural Foods, Inc. dba UNFI	4b78d0c8-7d0c-45e6-9b36-b248f002f2b8	2025-02-10	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
Equate Famotidine	FAMOTIDINE	Wal-Mart Stores Inc	15973213-0e11-4d18-b437-50b0a593cb7b	2025-02-06	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400
heartburn relief original strength	FAMOTIDINE	Proficient Rx LP	5567aaaf-b4f2-4604-b841-c9447e77256c	2019-10-01	Warnings	Exact identifier application applno (ANDA): 075400 application number: ANDA075400

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5QZO15J2Z8	FAMOTIDINE	76824-35-6	FAMOTIDINE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-031-65	11673003165	30 BLISTER PACK in 1 CARTON (11673-031-65) > 1 TABLET, FILM COATED in 1 BLISTER PACK	30 blister pack	2015-03-13	0000-00-00	No	No	Current
11673-031-72	11673003172	1 BOTTLE in 1 CARTON (11673-031-72) > 60 TABLET, FILM COATED in 1 BOTTLE	1 bottle	2022-01-26	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Target Corporation Famotidine Tablets, 10 mg Drug Facts	Target Corporation	2025-02-10	HUMAN OTC DRUG LABEL	6