Famotidine

Product NDC: 72205-145
Requested package NDC: 72205-145-99
11-digit product format: 722050145
Labeler code: 72205
Product ID: 72205-145_34acb853-6632-49cd-970a-e6fd840852d3
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Famotidine
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Novadoz Pharmaceuticals LLC
Application: ANDA217400
Marketing category: ANDA
Marketing start: 2024-08-06
Substance: FAMOTIDINE
Active strength: 20 mg/1
Pharmacologic classes: Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

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
A217400-001	FAMOTIDINE	FAMOTIDINE	20MG	TABLET / ORAL	AB		2024-08-06
A217400-002	FAMOTIDINE	FAMOTIDINE	40MG	TABLET / ORAL	AB		2024-08-06

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 2 matching rows.

Application-product, TE code table
Application-product	TE code
A217400-001	AB
A217400-002	AB

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.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`79d66fd596c7…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	A217400-001	FAMOTIDINE	20MG	TABLET / ORAL	AB	2024-08-06	`a50c72e98297…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	A217400-002	FAMOTIDINE	40MG	TABLET / ORAL	AB	2024-08-06	`a50c72e98297…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-09-14 22:38:34	2026-08	A217400-001	AB	1	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A217400-002	AB	1	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A217400-001	AB	1	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A217400-002	AB	1	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A217400-001	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A217400-002	AB	1	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A217400-001	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A217400-002	AB	1	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A217400-001	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A217400-002	AB	1	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A217400-001	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A217400-002	AB	1	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A217400-001	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A217400-002	AB	1	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A217400-001	AB	1	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A217400-002	AB	1	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A217400-001	AB	1	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A217400-002	AB	1	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A217400-001	AB	1	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A217400-002	AB	1	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A217400-001	AB	1	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A217400-002	AB	1	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A217400-001	AB	1	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A217400-002	AB	1	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A217400-001	AB	1	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A217400-002	AB	1	`79d66fd596c7…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	A217400-001	AB	1	`a50c72e98297…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	A217400-002	AB	1	`a50c72e98297…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Famotidine
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
FAMOTIDINE	20 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5QZO15J2Z8	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
284245	Internal RxNorm lookup
310273	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
74a24590-a0b6-4607-8e67-9fadce53389b	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
396bde5c-c78e-2f8b-ab1f-2ee6ba32bcae	Product name	7	20260317
1e73f975-1ce7-705e-2bcf-788b1b5e24ba	Product name	5	20251124
cf645750-2e70-f6e1-c05a-a52847def5dd	Product name	9	20250312
4fdc761c-585e-054b-8ebe-86130a26e4c1	Product name	2	20221205
fc2e1e31-353a-2c24-a4b4-fcf93bf7e38e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72205-145-05	Famotidine	500 in 1 BOTTLE	TABLET, FILM COATED	500	2
72205-145-30	Famotidine	30 in 1 BOTTLE	TABLET, FILM COATED	30	2
72205-145-50	Famotidine	50 in 1 BOTTLE	TABLET, FILM COATED	50	2
72205-145-91	Famotidine	100 in 1 BOTTLE	TABLET, FILM COATED	100	2
72205-145-98	Famotidine	75 in 1 BOTTLE	TABLET, FILM COATED	75	2
72205-145-99	Famotidine	1000 in 1 BOTTLE	TABLET, FILM COATED	1000	2

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72205-145-05	EA - Each	72205-145	4fb0618f-74a5-4f59-8210-cb4627c6c843	1	2025-02-10
72205-145-30	EA - Each	72205-145	0182f562-c049-48cd-b719-7cfe6b7a796d	1	2025-02-10
72205-145-91	EA - Each	72205-145	12d2f78c-9eb9-4e08-9274-5ae09a551013	1	2025-02-10
72205-145-99	EA - Each	72205-145	c841f6ff-c204-4564-96bb-8d67908c1e8b	1	2025-02-10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72205-145	FAMOTIDINE TABLET, FILM COATED [NOVADOZ PHARMACEUTICALS LLC]	1	Current NDC, 6 package rows	20240920_74a24590-a0b6-4607-8e67-9fadce53389b.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 · 8 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Famotidine	FAMOTIDINE	REMEDYREPACK INC.	669fbd46-cae5-4477-884e-8eca893d2e05	2026-09-09	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 217400 application number: ANDA217400
Famotidine	FAMOTIDINE	Preferred Pharmaceuticals Inc.	cd95271c-cf39-47fb-97a6-f6ee1e619e4a	2026-08-12	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 217400 application number: ANDA217400
Famotidine	FAMOTIDINE	Advanced Rx of Tennessee, LLC	5648ca13-1add-56ec-e063-6294a90a6f29	2026-07-10	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 217400 application number: ANDA217400
Famotidine	FAMOTIDINE	REMEDYREPACK INC.	8dbf43e0-856f-443b-b8a4-c69e006878ea	2026-04-24	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 217400 application number: ANDA217400
Famotidine	FAMOTIDINE	Redpharm Drug	44f3f63d-4522-91e4-e063-6394a90a6d1b	2025-12-02	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 217400 application number: ANDA217400
Famotidine	FAMOTIDINE	Novadoz Pharmaceuticals LLC	74a24590-a0b6-4607-8e67-9fadce53389b	2025-11-12	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 217400 application number: ANDA217400 ndc (package): 72205-145-99 ndc (product): 72205-145 ndc11 (package): 72205014599
Famotidine	FAMOTIDINE	Bryant Ranch Prepack	c133a9e1-ca48-4ee2-8768-01f44f5dd511	2025-10-14	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 217400 application number: ANDA217400
Famotidine	FAMOTIDINE	Preferred Pharmaceuticals Inc.	6edbd842-cf86-48a5-bc22-967620a2b5cb	2025-09-05	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 217400 application number: ANDA217400

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
310273	famotidine 20 MG Oral Tablet	PSN	8dbf43e0-856f-443b-b8a4-c69e006878ea	3
310273	famotidine 20 MG Oral Tablet	SCD	8dbf43e0-856f-443b-b8a4-c69e006878ea	3
310273	famotidine 20 MG Oral Tablet	PSN	74a24590-a0b6-4607-8e67-9fadce53389b	2
284245	famotidine 40 MG Oral Tablet	PSN	74a24590-a0b6-4607-8e67-9fadce53389b	2
310273	famotidine 20 MG Oral Tablet	SCD	74a24590-a0b6-4607-8e67-9fadce53389b	2
284245	famotidine 40 MG Oral Tablet	SCD	74a24590-a0b6-4607-8e67-9fadce53389b	2
310273	famotidine 20 MG Oral Tablet	PSN	44f3f63d-4522-91e4-e063-6394a90a6d1b	1
310273	famotidine 20 MG Oral Tablet	PSN	6edbd842-cf86-48a5-bc22-967620a2b5cb	1
310273	famotidine 20 MG Oral Tablet	PSN	c133a9e1-ca48-4ee2-8768-01f44f5dd511	1
310273	famotidine 20 MG Oral Tablet	SCD	44f3f63d-4522-91e4-e063-6394a90a6d1b	1
310273	famotidine 20 MG Oral Tablet	SCD	6edbd842-cf86-48a5-bc22-967620a2b5cb	1
310273	famotidine 20 MG Oral Tablet	SCD	c133a9e1-ca48-4ee2-8768-01f44f5dd511	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Sample	Exclude flag	Status
72205-145-99	72205014599	1000 TABLET, FILM COATED in 1 BOTTLE (72205-145-99)	2024-09-18	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Famotidine	Advanced Rx of Tennessee, LLC	2026-07-10	HUMAN PRESCRIPTION DRUG LABEL	1
Famotidine	REMEDYREPACK INC.	2026-04-24	HUMAN PRESCRIPTION DRUG LABEL	3
Famotidine	Redpharm Drug	2025-12-02	HUMAN PRESCRIPTION DRUG LABEL	1
Famotidine	Novadoz Pharmaceuticals LLC \| MSN LABORATORIES PRIVATE LIMITED	2025-11-12	Human Prescription Drug Label	2
Famotidine	Bryant Ranch Prepack	2025-10-14	HUMAN PRESCRIPTION DRUG LABEL	1
Famotidine	Preferred Pharmaceuticals Inc.	2025-09-05	HUMAN PRESCRIPTION DRUG LABEL	1