Home NDC 61715-064 Famotidine
Product NDC 61715-064
11-digit product format 617150064
Labeler code 61715
Product ID 61715-064_c72f6118-d58c-46ae-87b1-107a47113237
Type HUMAN OTC DRUG
Nonproprietary name famotidine
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Kinray
Application ANDA090283
Marketing category ANDA
Marketing start 2012-02-15
Marketing end 0000-00-00
Substance FAMOTIDINE
Active strength 20 mg/1
NDC exclude flag No
Listing certified through 2019-12-31
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 · 42 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 61715-064-25 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 61715-064-25 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 61715-064-25 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 61715-064-25 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 61715-064-25 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 61715-064-25 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 61715-064-25 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 61715-064-25 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 61715-064-25 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 61715-064-25 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 61715-064-25 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 61715-064-25 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 61715-064-25 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 61715-064-25 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 61715-064-25 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 61715-064-25 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 61715-064-25 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 61715-064-25 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 61715-064-25 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 61715-064-25 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 61715-064-25 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
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 A090283-001 FAMOTIDINE FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 A090283-002 FAMOTIDINE FAMOTIDINE 20MG TABLET / ORAL 2009-11-17
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 · 82 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 2026-02-19 14:30 UTC 2026-02 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 8072bd15b7f6…2024-05-31 18:47 UTC 2024-05 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 5c6f7cd8ea54…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 5d02ea3f76ae…2022-04-08 23:34 UTC 2022-04 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 4b0b4de00fa7…2022-04-04 05:41 UTC 2022-04 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 74a2ff9319b5…2019-12-13 00:20 UTC 2019-12 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 bb7c543d1eb4…2022-03-09 01:35 UTC 2022-03 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A090283-001 FAMOTIDINE 10MG TABLET / ORAL 2009-11-17 782e0a99824c…2021-12-28 21:50 UTC 2021-12 A090283-002 FAMOTIDINE 20MG TABLET / ORAL 2009-11-17 782e0a99824c…
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded FAMOTIDINE ACTIVE INGREDIENT 5QZO15J2Z8 FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 FAMOTIDINE ACTIVE MOIETY 5QZO15J2Z8 FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 COLLOIDAL SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 FERRIC OXIDE RED INACTIVE INGREDIENT 1K09F3G675 FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 HYDROXYPROPYL CELLULOSE INACTIVE INGREDIENT RFW2ET671P FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 STARCH, PREGELATINIZED CORN INACTIVE INGREDIENT O8232NY3SJ FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 TALC INACTIVE INGREDIENT 7SEV7J4R1U FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP FAMOTIDINE TABLET, FILM COATED [KINRAY] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61715-064 FAMOTIDINE TABLET, FILM COATED [KINRAY] 1 Legacy NDC 20130626_3545b503-bcc1-4ca3-83c6-abe04f87c6c6.zip