Famotidine

Product NDC
71821-010
11-digit product format
718210010
Labeler code
71821
Product ID
71821-010_0fc43ab9-0e23-258f-e063-6394a90a0c40
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
VKT Pharma Private Limited
Application
ANDA215822
Marketing category
ANDA
Marketing start
2022-01-28
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
Rxcui199047, 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
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718
4fdc761c-585e-054b-8ebe-86130a26e4c1Product name220221205
fc2e1e31-353a-2c24-a4b4-fcf93bf7e38eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71821-010-12Famotidine144230 in 1 BAGTABLET, FILM COATED1442304
71821-010-13Famotidine144230 in 1 BAGTABLET, FILM COATED1442301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71821-010FAMOTIDINE TABLET, FILM COATED [VKT PHARMA PRIVATE LIMITED]4Current NDC, Legacy NDC, 1 package rows20240126_4e5db906-992f-476b-9d97-63a4c582bbdc.zip
71821-010FAMOTIDINE TABLET, FILM COATED [VKT PHARMA PRIVATE LIMITED]1Current NDC, Legacy NDC, 1 package rows20240524_1c2cfb3c-eaa0-403f-9589-d706afc06f51.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199047famotidine 10 MG Oral TabletPSN4e5db906-992f-476b-9d97-63a4c582bbdc4
310273famotidine 20 MG Oral TabletPSN4e5db906-992f-476b-9d97-63a4c582bbdc4
199047famotidine 10 MG Oral TabletSCD4e5db906-992f-476b-9d97-63a4c582bbdc4
310273famotidine 20 MG Oral TabletSCD4e5db906-992f-476b-9d97-63a4c582bbdc4
199047famotidine 10 MG Oral TabletPSN1c2cfb3c-eaa0-403f-9589-d706afc06f511
310273famotidine 20 MG Oral TabletPSN1c2cfb3c-eaa0-403f-9589-d706afc06f511
199047famotidine 10 MG Oral TabletSCD1c2cfb3c-eaa0-403f-9589-d706afc06f511
310273famotidine 20 MG Oral TabletSCD1c2cfb3c-eaa0-403f-9589-d706afc06f511

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71821-010-1271821001012144230 TABLET, FILM COATED in 1 BAG (71821-010-12) 2022-09-070000-00-00NoNoCurrent
71821-010-1371821001013144230 TABLET, FILM COATED in 1 BAG (71821-010-13) 2024-05-23NoNoHistorical