FAMOTIDINE

Product NDC
67877-842
11-digit product format
678770842
Labeler code
67877
Product ID
67877-842_23381364-14e1-4f63-aea4-66d605fd14f1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FAMOTIDINE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Ascend Laboratories, LLC
Application
ANDA215630
Marketing category
ANDA
Marketing start
2022-07-08
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

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FAMOTIDINE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5QZO15J2Z8
Rxcui284245, 310273

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
396bde5c-c78e-2f8b-ab1f-2ee6ba32bcaeProduct name720260317
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
cf645750-2e70-f6e1-c05a-a52847def5ddProduct name920250312
4fdc761c-585e-054b-8ebe-86130a26e4c1Product name220221205
fc2e1e31-353a-2c24-a4b4-fcf93bf7e38eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67877-842-01FAMOTIDINE100 in 1 BOTTLETABLET, FILM COATED1005
67877-842-05FAMOTIDINE500 in 1 BOTTLETABLET, FILM COATED5005
67877-842-10FAMOTIDINE1000 in 1 BOTTLETABLET, FILM COATED10005

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67877-842-01EA - Each67877-842acf1127f-10b0-42f6-8d25-9d15a7f2f11612022-08-04
67877-842-05EA - Each67877-842f41db46f-768e-4f7c-b2b3-c7f9d6a68f1112025-02-10
67877-842-10EA - Each67877-842d3585909-1c28-4b80-a31c-8dc3cff2d25612022-08-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67877-842FAMOTIDINE TABLET, FILM COATED [ASCEND LABORATORIES, LLC]4Current NDC, Legacy NDC, 3 package rows20250131_be69d9f9-f4ad-4cfe-bab2-e07186b25c1e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310273famotidine 20 MG Oral TabletPSNa24e8f45-6ace-4a81-8005-c23a55dadd9a103
310273famotidine 20 MG Oral TabletSCDa24e8f45-6ace-4a81-8005-c23a55dadd9a103
310273famotidine 20 MG Oral TabletPSNe59a2c97-19c7-485c-bb1b-272ddb9ae05313
310273famotidine 20 MG Oral TabletSCDe59a2c97-19c7-485c-bb1b-272ddb9ae05313
310273famotidine 20 MG Oral TabletPSN3ab235f4-da59-4a92-ad6b-c76cf3ecd9855
310273famotidine 20 MG Oral TabletPSNfd271deb-c748-bf26-e053-6294a90a11aa5
310273famotidine 20 MG Oral TabletPSNbe69d9f9-f4ad-4cfe-bab2-e07186b25c1e5
284245famotidine 40 MG Oral TabletPSNbe69d9f9-f4ad-4cfe-bab2-e07186b25c1e5
310273famotidine 20 MG Oral TabletSCDbe69d9f9-f4ad-4cfe-bab2-e07186b25c1e5
310273famotidine 20 MG Oral TabletSCD3ab235f4-da59-4a92-ad6b-c76cf3ecd9855
310273famotidine 20 MG Oral TabletSCDfd271deb-c748-bf26-e053-6294a90a11aa5
284245famotidine 40 MG Oral TabletSCDbe69d9f9-f4ad-4cfe-bab2-e07186b25c1e5
310273famotidine 20 MG Oral TabletPSNb445a613-eaa8-45e8-be1f-5848bfd1dd364
310273famotidine 20 MG Oral TabletSCDb445a613-eaa8-45e8-be1f-5848bfd1dd364
310273famotidine 20 MG Oral TabletPSN3c32f8e2-f54a-422d-9c25-68692ea090013
310273famotidine 20 MG Oral TabletSCD3c32f8e2-f54a-422d-9c25-68692ea090013
310273famotidine 20 MG Oral TabletPSNfa1b16ed-2936-dc98-e053-6294a90acde82
310273famotidine 20 MG Oral TabletSCDfa1b16ed-2936-dc98-e053-6294a90acde82
310273famotidine 20 MG Oral TabletPSN69bd5340-298b-46ca-83c7-0b5ef233f9c51
310273famotidine 20 MG Oral TabletPSN74a69baa-a7c5-4e67-8db6-2ec39ab6cfe51
284245famotidine 40 MG Oral TabletPSN69bd5340-298b-46ca-83c7-0b5ef233f9c51
310273famotidine 20 MG Oral TabletSCD69bd5340-298b-46ca-83c7-0b5ef233f9c51
310273famotidine 20 MG Oral TabletSCD74a69baa-a7c5-4e67-8db6-2ec39ab6cfe51
284245famotidine 40 MG Oral TabletSCD69bd5340-298b-46ca-83c7-0b5ef233f9c51

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
67877-842-0167877084201100 TABLET, FILM COATED in 1 BOTTLE (67877-842-01) 2022-07-080000-00-00NoNoCurrent
67877-842-0567877084205500 TABLET, FILM COATED in 1 BOTTLE (67877-842-05) 2025-02-03NoNoCurrent
67877-842-10678770842101000 TABLET, FILM COATED in 1 BOTTLE (67877-842-10) 2022-07-080000-00-00NoNoCurrent